Image MitochondrialDNA en.svg thumb 300px right Human mitochondrialDNA. File Electron microscopy reveals mitochondrialDNA in discrete foci.jpg thumb Electron microscopy reveals mitochondrialDNA in discrete ... www.biomedcentral.com 1741 7007 2 9 ref MitochondrialDNA mtDNA is the DNA located in organelles called ... organisms is found in the cell nucleus . MitochondrialDNA can be regarded as the smallest ... John JC, Facucho Oliveira J, Jiang Y, Kelly R, Salah R title MitochondrialDNA transmission, replication ... 20231166 doi 10.1093 humupd dmq002 url ref Origin Nuclear and mitochondrialDNA are thought to be of separate ... by exponential polymerase chain reaction, copy number of mitochondrialDNA in rat tissues journal ... a sperm into an oocyte , may interfere with this. The fact that mitochondrialDNA is maternally ... or HVR2 of the mitochondrialDNA, as with a genealogical DNA test . HVR1 consists of about 440 base ... inheritance of Mytilus mitochondrialDNA journal Science volume 251 pages 1488 1490 pmid 1672472 ..., Moritz RF title Transfer of paternal mitochondrialDNA during fertilization of honeybee Apis mellifera ... of mitochondrialDNA in mice journal Nature volume 352 issue 6332 pages 255 7 year 1991 pmid 1857422 ... W, et al. title Further evidence for paternal inheritance of mitochondrialDNA in the sheep Ovis aries ... al. title Composition of parental mitochondrialDNA in cloned bovine embryos journal FEBS Lett. volume ... inheritance of mitochondrialDNA journal N. Engl. J. Med. volume 347 issue 8 pages 576 80 year 2002 ... of mitochondrialDNA varies among species. Information in this section is specific to human mitochondrialDNA Electron transport chain The mitochondrial genome contains 13 protein coding genes. Many ... center Valine Val V MT TV mitochondrial MT TV Mutations File MitochondrialDNA and diseases.png thumb The involvement of mitochondrialDNA in several human diseases. Susceptibility mtDNA is particularly ... L. title MitochondrialDNA and aging journal Clinical Science volume 107 pages 355 364 date July 2004 ... more details
Orphan date September 2010 Infobox Journal title MitochondrialDNA editor Rob DeSalle discipline CellBiology ... CODEN ISSN 1940 1736 eISSN 1940 1744 MitochondrialDNA is an academic journal that publishes Review journal review articles on the current and developing technologies around mitochondrialDNA research ... and Scope Previously published under the title DNA Sequence Vols 1 19.3 , MitochondrialDNA accepts original high quality reports based on mapping, sequencing and analysis of mitochondrialDNA and RNA. Descriptive papers on DNA sequences from mitochondrial genomes, and also analytical papers in the areas of population genetics, medical genetics, phylogenetics and human evolution that use mitochondrialDNA as a source of evidence for studies will be considered for publication. The editorial board ... address the use of mitochondrialDNA sequences, as well as papers that discuss the utility of mitochondrialDNA information in medical studies and in human evolutionary biology. Editor in Chief http desalle.amnh.org Rob DeSalle American Museum of Natural History is the Editor in Chief of MitochondrialDNA ref cite web url http www.informahealthcare.com page EditorialAdvisoryBoard?journalCode ... http informahealthcare.com toc mdn 22 S1 ref Publication Format MitochondrialDNA publishes WebFirst ... Scopus Zoological Record . References reflist 2 External links http www.informahealthcare.com mdn MitochondrialDNA homepage of MitochondrialDNA Category Publications established in 1980 Category Genetics ... Discovery and description of mitochondrial genome sequences Structure and function of mtDNA genes and genomic ... koloko.net Sergios Orestis Kolokotronis Barnard College, Columbia University . Special Issues MitochondrialDNA has published so far two special free access issues on DNA Barcoding Mexican Barcode of Life ... to the online version is included in all subscriptions. Abstracting & Indexing MitochondrialDNA is abstracted in Current Contents Life Sciences Science Citation Index Research Alert Elsevier BIOBASE ... more details
America at the far right. Migration patterns are based on studies of mitochondrial matrilinear DNA ... references External links Mitochondrial Phylogenetic Trees Ian Logan s http www.ianlogan.co.uk mtDNA.htm MitochondrialDNA Site Mannis van Oven s http www.phylotree.org PhyloTree.org cite journal author .... Image Migration map4.png thumb right 350px Another model of human migration based on MitochondrialDNA In human genetics , a human mitochondrialDNA haplogroup is a haplogroup defined by differences in Human mitochondrial genetics human mitochondrialDNA . Haplogroups are used to represent the major branch points on the mitochondrial phylogenetic tree. Understanding the evolutionary path of the female ... humans . She is commonly called Mitochondrial Eve . genetic genealogy Evolutionary relationship ... van Oven M, Kayser M title Updated comprehensive phylogenetic tree of global human mitochondrialDNA variation journal Human Mutation volume 30 issue 2 pages E386 94 year 2009 month February pmid 18853457 doi 10.1002 humu.20921 ref and subsequent published research. Macro haplogroup L mtDNA L Mitochondrial ... of Eve Bryan Sykes had claimed there were seven major mitochondrial lineages for modern Europeans ... DNA test Genetic Genealogy MtDna haplogroups by populations Human Y chromosome DNA haplogroups Genetics Human mitochondrial molecular clock Cambridge Reference Sequence haplogroup Human mitochondrial ... 08 02.jpg Mitochondrial haplogroup skeleton Vincent Macaulay s http www.stats.gla.ac.uk vincent founder2000 motif.html Mitochondrial haplogroup motifs Cambridge DNA s https www.cambridgedna.com genealogy dna ancient migrations slideshow.php An mtDNA view of the peopling of the world by Homo ... pdf 43026 doron.pdf Commons category Human mtDNA haplogroups DEFAULTSORT Human MitochondrialDna Haplogroup Category Human mtDNA haplogroups Category Genetic genealogy Category Recent single ... lidsk mitochondri ln DNA es Haplogrupos de ADN mitocondrial humano ko DNA hi ... more details
As a logical conclusion of the endosymbiotic theory , since modern day mitochondrial and chloroplast genomes do not contain a full set of housekeeping genes, and lack many that other descendants of their speculative ancestors share, there must have been a loss of genes. However, some of these genes likely migrated to the nucleus, where analogues of these genes are now found. Puzzle It is not clear why only a subset of genes have been transferred, when such gene transfer is known to be rapid on a similar timescale as mutation. Mitochondria and chloroplasts perform redox reactions, which are known to be considerably mutagenic . Such mutagenicity would encourage migration of genes away from the organelles to the nucleus. Proposed explanations Since chloroplast and mitochondrial genetic code s differ slightly from the eukaryotic nuclear code, some genes may lose function when they are transferred. References Allen, J. F., Puthiyaveetil, S., Str m, J. & Allen, C. A. 2005. BioEssays 27 426 435. de Grey, A. D. N. J. 2005. Forces maintaining organellar genomes is any as strong as genetic code disparity or hydrophobicity? BioEssays 27 436 446. See also Human mitochondrial genetics MitochondrialDNA CoRR Hypothesis Category Genetics Category Mitochondrial genetics ... more details
Mitochondria can divide by fission and since they require mitochondrialDNA for their function, fission is coordinated with MitochondrialDNA Replication DNA replication . Some of the proteins that are involved in mitochondrial fission have been identified and some of them are associated with mitochondrial disease s. ref Cite pmid 21776419 ref Mechanism The DNM1L Drp1 protein is a member of the Dynamin family of large GTPases . Drp1 controls the final part of mitochondrial fission, pinching off the membrane stalk between two forming daughter mitochondria. The MFN2 protein is part of a complex that links the endoplasmic reticulum ER to mitochondria. Points of ER mitochondrial association have been associated with the formation of Drp1 complexes and mitochondrial fission. ref Cite pmid 21885730 ref Several Drp1 binding proteins have been identified. ref Cite pmid 21772324 ref A protein called mitochondrial fission factor Mff binds Drp1 and promotes mitochondrial fission. ref Cite pmid 21149567 ref The FIS1 protein might recruit Drp1 to sites of fission ref Cite pmid 21647385 ref but it might require association with another protein, MIEF1 coded for by the SMCR7L gene , to promote mitochondrial fission. In contrast, MIEF1 when bound to Drp1 might prevent mitochondrial fission and thus shift the balance towards fusion of mitochondria. ref Cite pmid 21701560 ref References reflist Category Mitochondria ... more details
Mitochondrial biogenesis is the process by which new mitochondria are formed in the cell. Mitochondrial biogenesis is activated by numerous different signals during times of cellular stress or in response to environmental stimuli. The mitochondrion is a key regulator of the metabolic activity of the cell, and is also an important organelle in both production and degradation of free radicals. It is thought that higher mitochodrial copy number or higher mitochondrial mass is protective for the cell. Mitochondria are produced from the transcription and translation of genes both in the nuclear genome and in the MitochondrialDNAmitochondrial genome . The majority of mitochondrial protein comes from the nuclear genome, while the mitochondrial genome encodes most parts of the electron transport chain along with mitochondrial rRNA and tRNA . A major adaptation to mitochondrial biogenesis results in more mitochondrial tissues which increases metabolic enzymes for glycolysis, oxidative phosphorylation and ultimately a greater mitochondrial metabolic capacity. Peter D. Wagner Summer 2011 Lecture cn date October 2011 The master regulators of mitochondrial biogenesis appear to be the peroxisome proliferator activated receptor gamma PGC family of transcriptional coactivators, including PPARGC1A PGC 1 , PPARGC1B PGC 1 , and the PGC related coactivator, PRC. PGC 1 , in particular, is thought to be a master regulator. It is known to co activate nuclear respiratory factor 2 GABPA NRF2 GABPA , and together with NRF 2 coactivates nuclear respiratory factor 1 NRF1 . The NRFs, in turn, activate the mitochondrial transcription factor A TFAM tfam , which is directly responsible for transcribing nuclear encoded mitochondrial proteins. This includes both structural mitochondrial proteins as well as those involved in Human mitochondrial genetics Replication.2C repair.2C transcription.2C and translation mtDNA transcription, translation, and repair . See also mitochondria References Unreferenced ... more details
ATP that powers most cell functions. Mitochondrial diseases are often caused by genetics or mutations to the mitochondrialDNA that affect mitochondria function. Mitochondrial diseases take on unique ... of the defective mitochondrialDNA may vary from organ to organ within the body, and each mutation is modulated ... DNA mtDNA or in nuclear genes that code for mitochondrial components. They may also be the result ... causes see Medical Subject Headings MeSH . MitochondrialDNA inheritance behaves differently ... DNA, however, is strictly inherited from the mother and each mitochondrial organelle typically contains multiple mtDNA copies see Heteroplasmy . During cell division the mitochondrialDNA copies ... threshold expression . MitochondrialDNA mutations occur frequently, due to the lack of the error checking capability that nuclear DNA has see Mutation rate . This means that mitochondrialDNA ... DNA replication all of which are encoded for by genes in the nuclear DNA may also cause mitochondrialDNA mutations. Most mitochondrial function and biogenesis is controlled by nuclear DNA . Human mitochondrial ... the defective mitochondrialDNA behind, is a potential treatment procedure that has been successfully ... transplanted healthy DNA in human eggs from women with mitochondrial disease into the eggs of women ... to prevent transmission of mitochondrialDNA disease journal Nature volume 465 issue 7294 pages 82 85 ...Unreferenced section date December 2011 Infobox Disease Name Mitochondrial disease Image Ragged red fibres gtc very high mag.jpg Caption Micrograph showing ragged red fibres, a finding seen in mitochondrial ... Mitochondrial diseases are a group of disorders caused by dysfunctional mitochondria , the organelle ... symptoms are often called a mitochondrial myopathy . There is some evidence for mitochondrial dysfunction as the molecular basis of bipolar disorder. In addition, classical mitochondrial diseases occur in a subset of individuals with autism and are usually caused by genetic anomalies or mitochondrial ... more details
Infobox Disease Name Mitochondrial encephalomyopathy Image Caption DiseasesDB ICD10 ICD9 ICD9 277.87 ICDO OMIM MedlinePlus eMedicineSubj eMedicineTopic MeshID D017237 A Mitochondrial encephalomyopathy is a form of encephalomyopathy that is associated with a mitochondrial disease . Examples include Mitochondrial encephalomyopathy, lactic acidosis, and stroke like episodes MELAS and MERRF syndrome MERRF . These conditions can sometimes present together. ref name pmid14967777 cite journal author Melone MA, Tessa A, Petrini S, et al title Revelation of a new mitochondrialDNA mutation G12147A in a MELAS MERFF phenotype journal Arch. Neurol. volume 61 issue 2 pages 269 72 year 2004 month February pmid 14967777 doi 10.1001 archneur.61.2.269 url http archneur.ama assn.org cgi pmidlookup?view long&pmid 14967777 ref ref name pmid15767514 cite journal author Naini AB, Lu J, Kaufmann P, et al title Novel mitochondrialDNA ND5 mutation in a patient with clinical features of MELAS and MERRF journal Arch. Neurol. volume 62 issue 3 pages 473 6 year 2005 month March pmid 15767514 doi 10.1001 archneur.62.3.473 url http archneur.ama assn.org cgi pmidlookup?view long&pmid 15767514 ref Kearns Sayre syndrome KSS is sometimes included in this category, ref name pmid8350109 cite journal author Crimmins D, Morris JG, Walker GL, et al title Mitochondrial encephalomyopathy variable clinical expression within a single kindred journal J. Neurol. Neurosurg. Psychiatr. volume 56 issue 8 pages 900 5 year 1993 month August pmid 8350109 pmc 1015147 doi 10.1136 jnnp.56.8.900 url http jnnp.bmj.com cgi pmidlookup?view long&pmid 8350109 ref but it is not included in this category in Medical Subject Headings MeSH . References reflist 2 Mitochondrial diseases Category Neurotrauma disease stub zh ... more details
Expert subject Biology date November 2009 No footnotes date May 2011 Mitochondrial decay is one major cause of aging , leading to the subsequent death in humans. The mitochondria are the power producing organelles found in every cell of every organ. Their primary function is to generate Adenosine triphosphate ATP through various energy cycles that involve nutrients and vitamins. ATP is needed for every movement, thought and action we make. Yet very little ATP can be stored in the body. Under normal conditions the mitochondria generate free radicals during the ATP production process and as a result subject themselves to a lot of free radical damage. As we age, the mitochondria become less efficient, fewer in number and larger. Accordingly, ATP production declines, and this may eventually lead to cell death. As organs cannot borrow energy from one another, the efficiency of each organ s mitochondria is essential to its repair processes and functions. If an organ s mitochondria fail, then so does that organ. Enhancement and protection of mitochondrial function and structure are therefore instrumental in preventing and slowing aging. Mitochondrial decay is a progressive disruption of mitochondrial structural integrity and functional ability with advancing age. It can cause impairment in cellular energy production and hence a decline in normal function, particularly in organs with high energy consumption such as the brain and the heart. Mitochondrial decay can also lead to an increase in free radical production and thus render a cell more prone to commit suicide programmed cell death or apoptosis . Some of the age related diseases, including cardiovascular and neurodegenerative disorders, have been found to involve mitochondrial dysfunction. The maintenance of a youthful mitochondrial functional ability and antioxidant capacity has become a trend in preventive health. Reference RK Lab http www.rk lab.com Category DNA Category Aging ... more details
Human mitochondrialDNA haplogroup Mitochondrial macro haplogroups Haplogroup L0 mtDNA L0 ... all mitochondrialDNA mtDNA is generally passed from mother to offspring without recombination biology recombination , all mitochondrialDNA mtDNA in every living person is directly descended from ... further Genetic genealogy matrilineal MitochondrialDNA Human mitochondrial molecular clock File ... 250px Simplified Human mitochondrial phylogeny Without a DNA sample, it is not possible to reconstruct ... DNA, however, parts of ancestral genomes are estimated by scientists. MitochondrialDNA mtDNA ... title Maternal inheritance of human mitochondrialDNA journal PNAS volume 77 issue 11 pages 6715 ... give a mitochondrialDNA signature or haplotype e.g. the Cambridge Reference Sequence CRS is a haplotype ... mutation . Scientists sort mitochondrialDNA results into more or less related groups, with more or less ... of mitochondrialDNA between different people can be used to estimate the time back to a common ancestor ... at least one male, who do not pass on their mother s mitochondrialDNA, thereby breaking the line ... back to a MRCA however this MRCA is valid only when discussing mitochondrialDNA. An approximate ... Reed Friedlaender Ehret 2009 using data from many loci not just mitochondrialDNA extrapolated that the Angola ... study was considered by the authors to be broadly consistent with a previous mitochondrialDNA ... mitochondrialDNA haplogroups Col 3 Last universal ancestor Mitochondrial genome Neutral theory ... of major human mitochondrialDNA haplogroup expansions in Africa journal Proceedings. Biological Sciences ... of human mitochondrialDNA sequence variation. journal Proc Biol Sci. year 2009 volume 276 ... first1 D citation last1 Brown first1 WM title Polymorphism in mitochondrialDNA of humans as revealed ... first1 RL last2 Stoneking first2 M last3 Wilson first3 AC title MitochondrialDNA and human evolution ... of human mitochondrialDNA journal Mol. Biol. Evol. volume 9 issue 6 pages 1176 8 year 1992 month ... more details
pH difference across the outer mitochondrial membrane measured with a green fluorescent protein ... or TCA cycle takes place within the mitochondrial matrix. Prior to the citric acid cycle, pyruvic ... of the inner mitochondrial membrane. The NADH and FADH sub 2 sub produced by the citric acid ... chain. The protons return to the mitochondrial matrix through the process of chemiosmosis through the protein ATP synthase . See also Matrix biology References Reflist Mitochondrial enzymes DEFAULTSORT Mitochondrial Matrix Category Cell anatomy ca Matriu mitocondrial cs Mitochondri ln matrix ... more details
Image A DNA orbit animated small.gif right frame The A DNA structure. A DNA is one of the many possible double helical structures of DNA . A DNA is thought to be one of three biologically active double helical structures along with B DNA B and Z DNA . It is a right handed double helix fairly similar to the more common and well known B DNA form, but with a shorter more compact helical structure. It appears likely that it occurs only in dehydrated samples of DNA, such as those used in crystallographic experiments, and possibly is also assumed by DNA RNA hybrid helices and by regions of double stranded RNA. Structure A DNA is fairly similar to B DNA given that it is a right handed double helix with major ... turn. This results in a deepening of the major groove and a shallowing of the minor. Predicting A DNA structure An algorithm for predicting the propensity of a sequence to flip from B DNA to A DNA ... cite journal author Basham B, Schroth GP, Ho PS title An A DNA triplet code thermodynamic rules for predicting A and B DNA journal Proc Natl Acad Sci USA volume 92 issue 14 pages 6464 6468 year ... in the hydration of DNA surfaces can be used to distinguish between sequences that form A and B DNA. From this, a triplet code of A DNA propensities was derived as energetic rules for predicting A DNA formation. This code correctly predicted 90 of A and B DNA sequences in crystals and correlates with A DNA formation in solution. Thus, with our previous studies on Z DNA, we now have a single method to predict the relative stability of sequences in the three standard DNA duplex conformations. ref name Basham1995 blockquote Comparison Geometries of the Most Common DNA Forms Image A DNA, B DNA and Z DNA.png right thumb Side view of A , B , and Z DNA. Image B&Z&A DNA formula.jpg thumb right 250px The helix axis of A , B , and Z DNA. class wikitable Geometry attribute A form B form Z form Helix ... also Mechanical properties of DNADNA B DNA Z DNA External links http www.tulane.edu biochem nolan ... more details
Introduction to genetics Other uses File DNA Structure Key Labelled.pn NoBB.png thumb right 340px The structure of the DNA double helix . The atoms in the structure are colour coded by element and the detailed ... of part of a DNA double helix Deoxyribonucleic acid IPAc en audio en us Deoxyribonucleic acid.ogg d i k s i r a b . n ju k l e . k s d DNA is a nucleic acid containing ... s with the exception of RNA virus es . The DNA segments carrying this genetic information are called gene s. Likewise, other DNA sequences have structural purposes, or are involved in regulating the use of this genetic information. Along with RNA and proteins , DNA is one of the three major macromolecules that are essential for all known forms of life. DNA consists of two long polymers of simple ... stretches of DNA into the related nucleic acid RNA in a process called transcription genetics transcription . Within cells DNA is organized into long structures called chromosome s. During cell division these chromosomes are duplicated in the process of DNA replication , providing each cell ... , and protist s store most of their DNA inside the cell nucleus and some of their DNA in organelle s, such as mitochondria ... and archaea store their DNA only in the cytoplasm . Within the chromosomes, chromatin proteins such as histone s compact and organize DNA. These compact structures guide the interactions between DNA and other proteins, helping control which parts of the DNA are transcribed. Properties File DNA chemical structure.svg thumb 300px Chemical structure of DNA. Hydrogen bond s shown as dotted lines. DNA is a long polymer made from repeating units called nucleotide s. ref cite book last Saenger ... title Forensic DNA Typing publisher Elsevier isbn 978 0 12 147951 0 oclc 223032110 45406517 pp. 14 15. ref As first discovered by James D. Watson and Francis Crick , the structure of DNA of all species ... to another study, when measured in a particular solution, the DNA chain measured 22 to 26 ngstr m ... more details
Symptomatic overlap with other mitochondrial myopathies References reflist Diseases of myoneural junction and muscle Mitochondrial diseases Category Myoneural junction and neuromuscular diseases Category Mitochondrial diseases zh ... more details
Mitochondrial toxicity is a condition in which the mitochondrion mitochondria of a body s cells become damaged or decline significantly in number it occurs as a side effect of certain antiretroviral drug s used to treat human immunodeficiency virus, or HIV . Causes While the exact causes of mitochondrial toxicity are not known, research has shown that a certain group of anti viral drugs used to treat HIV, specifically nucleoside analog reverse transcriptase inhibitor s NRTIs , interfere with an enzyme needed in the production of mitochondria. ref http www.thebody.com pinf mitochondrial.html ref Symptoms The disruption of cell function that accompanies the condition can cause both mild and severe problems in people suffering from mitochondrial toxicity. The most commonly observed symptom is muscle weakness, or myopathy . Others include peripheral neuropathy numbness in the fingers and toes and pancreatitis inflammation of the pancreas , with the most severe being lactic acidosis , in which a build up of lactic acid in the tissues of the body leads to loss of energy, organ failure, and eventually death. ref http www.projinf.org fs mito b.html ref References references External links Mitochondrial toxicity at http www.hivnet.org OverHivEnAids Alternatief BrochureBijwerkingenEngels Mitochondrial 20toxicity.htm hiv.org Category Toxicology medical stub med toxic stub sl Mitohondrijska toksi nost ... more details
episode episodes 3 episode list Infobox animanga Footer nihongo DNA D N A D En Ei ..., spanning a total of five tank bon volumes. DNA was adapted into a 12 episode anime television ... and animation director for the series was Kumiko Takahashi . DNA has been broadcast in Japan by Animax ... children that carry the Mega Playboy DNA, causing them and all their descendants to each have 100 ... to deal with. Karin reveals to Junta that she is a DNA Operator . Her job is to make alterations in people s DNA that will change their nature for the greater good of society. She intends to shoot the original Mega Playboy with a DCM DNA Control Medicine bullet that will alter his DNA in order ... Playboy DNA stabilizes more and more. nihongo Karin Aoi Aoi Karin anime voices Miina Tominaga Jessica Calvello A sixteen year old DNA Operator from the overcrowded future, sent back in time in order ... The DNA manga was published in Japanese magazine Weekly Sh nen Jump 1993 No. 36 through 1994 No. 29 ... Category Sh nen manga Link GA es ca DNA cs DNA de DNA es DNA fr DNA ko DNA id DNA it DNA ja D N A pt DNA ru DNA fi DNA sv DNA tl DNA zh DNA ... more details
Pfam box Symbol Mito carr Name image 1okc opm.gif width 220 caption Mitochondrial ADP ATP carrier Pfam PF00153 InterPro IPR001993 SMART PROSITE PDOC00189 SCOP 1okc TCDB 2.A.29 OPM family 21 OPM protein 1okc PDB PDB3 2bmn A 9 104 PDB3 2c3e A 112 206 PDB3 1ymj A 112 206 PDB3 1okc A 112 206 PDB3 1ym6 A 112 206 Mitochondrial carriers are proteins from the solute carrier family which transfers molecules across the membranes of the mitochondria . ref name Nury 2006 cite journal author Nury H, Dahout Gonzalez C, Tr z guet V, Lauquin GJ, Brandolin G, Pebay Peyroula E title Relations between structure and function of the mitochondrial ADP ATP carrier journal Annu. Rev. Biochem. volume 75 issue pages 713 ... mitochondrial membrane inner membranes of mitochondria and other eukaryotic organelles such as the peroxisome ... author Walker JE title The mitochondrial transporter family journal Curr. Opin. Struct. Biol. volume ... journal author Kuan J, Saier Jr MH title Expansion of the mitochondrial carrier family journal Res ... Site directed mutagenesis of the yeast mitochondrial ADP ATP translocator. Six arginines and one lysine ... 10.1006 jmbi.1993.1233 ref ref name PUB00001675 cite journal author Palmieri F title Mitochondrial ... B title PMP47, a peroxisomal homologue of mitochondrial solute carrier proteins journal Trends ... transport protein Graves disease carrier protein yeast mitochondrial proteins MRS3 and MRS4 yeast mitochondrial FAD carrier protein and many others. Structure All mitochondrial carriers are encoded by nuclear ... the members of the mitochondrial carrier family that have been identified, it is the ADP ATP carrier ... of ADP ATP carrier translocation across the outer mitochondrial membrane journal J. Biol. Chem. volume ... dynamics of the mitochondrial ADP ATP carrier revealed by molecular dynamics simulation studies journal ... pdbe apps quips?story ATPexchange Getting a good rate of exchange the mitochondrial ADP ATP carrier ... families Category Transmembrane proteins membrane protein stub Membrane transport proteins Mitochondrial ... more details
Infobox album See Wikipedia WikiProject Albums Name Mitochondrial Blues Type Album Artist Noah23 Cover Noah23 mitochondrial blues.jpg Released July 27, 2004 Recorded 2003 2004 Genre Hip hop music Hip hop Length 56 26 Label Legendary Entertainment br Noah23 Plague Language Producer Blue Sky Black Death Orphan , Sseleman, Noah23 , Andrew H, DMS, Krinjah, King Champion, Naught, Dustmite Last album Ancient Israelites Older Than Anorthosite br 2004 This album Mitochondrial Blues br 2004 Next album Sigma Octantis album Sigma Octantis br 2004 Mitochondrial Blues is a 2004 album by hip hop artist Noah23 . This album was released simultaneously with Sigma Octantis album Sigma Octantis , as both albums are the product of the same recording sessions as Noah s higher profile 2004 album Jupiter Sajitarius . Track listing Silicate Magma Chamber Crunch Search and Destroy Harvest Remix Orange Dolphin Pure Vibes ft. Fake Four Inc Ceschi & Troubadour Twist of Fate ft. Baracuda rapper Baracuda Homewood ft. Feelix Enterworld ft. B One & Vex Bliss TS4 Freestyle Mechanical Bull ft. Baracuda Yed Posterior ft. Erosadis, Hangnail & Homesick Dustmite Data Hooks ft. Baracuda Drowning in You ft. AnuCongo Trilateral Damage ft. Orko the Sykotik Alien & StapleMouth Production credits Tracks 1, 5, 7, 14 & 16 produced by Blue Sky Black Death Orphan Tracks 6, 9 & 15 produced by Sseleman Track 2 produced by Noah23 as Warhol Track 3 produced by Andrew H Track 4 produced by DMS Track 8 produced by Krinjah Track 11 produced by King Champion Track 12 produced by Naught Track 13 produced by Dustmite Category 2004 albums Category Noah23 albums 2000s hiphop album stub ... more details
Orphan date December 2010 PBB geneid 94033 Mitochondrial ferritin is a ferroxidase enzyme that in humans is encoded by the FTMT gene . ref name pmid11323407 cite journal author Levi S, Corsi B, Bosisio M, Invernizzi R, Volz A, Sanford D, Arosio P, Drysdale J title A human mitochondrial ferritin encoded by an intronless gene journal J. Biol. Chem. volume 276 issue 27 pages 24437 40 year 2001 month July pmid 11323407 doi 10.1074 jbc.C100141200 url issn ref It is classified as a metal binding protein which is located within the mitochondrion mitochondria . After the protein is taken up by the mitochondria it can be processed into a mature protein and assemble functional ferritin shells. Structure Its structure was determined at 1.70 through the use of X ray diffraction and contains 182 residues. It is 67 helical. The Ramachandran plot shows that the structure of mitochondrial ferritin is mainly alpha helical with a low prevalence of beta sheets. References reflist 2 Further reading refbegin 2 cite journal author Langlois d Estaintot B, Santambrogio P, Granier T, et al. title Crystal structure and biochemical properties of the human mitochondrial ferritin and its mutant Ser144Ala. journal ... in HeLa cells are rescued by the expression of human mitochondrial ferritin. journal Biochim. Biophys ... author Cazzola M, Invernizzi R, Bergamaschi G, et al. title Mitochondrial ferritin expression in erythroid ... R, et al. title Mitochondrial ferritin a new player in iron metabolism. journal Blood Cells Mol. Dis ... P, et al. title Mitochondrial ferritin limits oxidative damage regulating mitochondrial iron ... EL, Ray PD, Tsuji Y title Role and regulation of ferritin H in rotenone mediated mitochondrial ... P, Levi S, et al. title Unique iron binding and oxidation properties of human mitochondrial ... SM, et al. title Mitochondrial ferritin in the substantia nigra in restless legs syndrome. journal ... 10.1097 NEN.0b013e3181bdc44f refend DEFAULTSORT Mitochondrial Ferritin Category EC 1.16.3 Category ... more details
The mitochondrial shuttles are systems used to transport reducing agents across the inner mitochondrial membrane . NADH cannot cross the membrane, but it can reduce another molecule that can cross the membrane, so that its electrons can reach the electron transport chain . The two main systems in humans are class wikitable Name In, to mitochondrion To electron transport chain ETC Out, to cytosol Glycerol phosphate shuttle glycerol 3 phosphate Coenzyme Q QH sub 2 sub 2 ATP dihydroxyacetone phosphate Malate aspartate shuttle malate Nicotinamide adenine dinucleotide NADH 3 ATP oxaloacetate ref name ufp Silva, Pedro. http www2.ufp.pt pedros bq respi.htm The chemical logic behind... Fermentation and Respiration , Universidade Fernando Pessoa , 2002 01 04. Retrieved on 2009 04 02. ref aspartate In humans, the glycerol phosphate shuttle is primarily found in brown adipose tissue , as the conversion is less efficient, thus generating heat, which is one of the main purposes of brown fat. It is primarily found in babies, though it is present in small amounts in adults around the kidneys and on the back of our necks. ref name ufp The malate aspartate shuttle is found in much of the rest of the body. Notes and references reflist Category Cellular respiration biochem stub ca Llan adora mitocondrial zh ... more details
inline date April 2010 Human mitochondrial genetics is the study of the genetics of the DNA contained ... to use, and are hence referred to as the powerhouses of the cell. MitochondrialDNA mtDNA is not transmitted through nuclear DNA nDNA . In humans, as in most multicellular organisms, mitochondrialDNA ... of mitochondrialDNA genetic code codes for functional mitochondrial proteins, and therefore most mitochondrial ... in mitochondrialDNA, or nuclear DNA coding for mitochondrial components. Slight problems with any ... lead to a number of diseases. Genome see MitochondrialDNAMitochondrialDNA mtDNA is present in mitochondria ... about 13 of them are coded on the mitochondrialDNA. Most of the 3000 proteins are involved in a variety ... the origins of replication of both heavy and light strands. The entire human mitochondrialDNA ... of nucleotides of a human mitochondrialDNA molecule 16,569 , as much as 0.42 of the mtDNA varies ... mitochondrial and nuclear DNA communicate and interact, even seemingly simple inheritance is hard to diagnose ... factors which may favor mutant or wildtype mitochondrialDNA, the threshold expression number of mtDNA ... to make as many mitochondria as that particular cell needs at the time. Human mitochondrialDNA ... of the complicated changes that the mRNA undergoes before it is translated. MitochondrialDNA polymerase The MitochondrialDNA Polymerase Pol gamma, encoded by the POLG gene is used in the copying of mtDNA ... error MitochondrialDNA is susceptible to damage from free radicals free oxygen radicals ... often caused by radicals created by defective proteins made from nuclear DNA. Mitochondrial diseases ... to inherited rather than acquired mutations of mitochondrialDNA. A given mitochondrial mutation can ... caused by abnormalities in mitochondrialDNA, many diseases are suspected to be associated in part ... in the aging aging process . See also Paternal mtDNA transmission Human mitochondrialDNA haplogroups Cambridge Reference Sequence Human mitochondrial molecular clock Genetic genealogy DNA databases ... more details
protein Name mitochondrially encoded tRNA valine caption image width HGNCid 7500 Symbol MT TV AltSymbols MTTV EntrezGene 4577 OMIM RefSeq NC 001807 UniProt PDB ECnumber Chromosome MT Arm Band LocusSupplementaryData Mitochondrially encoded tRNA valine also known as MT TV is a transfer RNA which in humans is encoded by the mitochondrion mitochondrial MT TV gene . ref name pmid7219534 cite journal author Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJ, Staden R, Young IG title Sequence and organization of the human mitochondrial genome journal Nature volume 290 issue 5806 pages 457 65 year 1981 month April pmid 7219534 doi 10.1038 290457a0 url ref MT TV is a small 69 nucleotide RNA human mitochondrial map position 1602 1670 that transfers the amino acid valine to a growing polypeptide chain at the ribosomal ribosome site of protein synthesis during translation genetics translation . References Reflist External links http www.ncbi.nlm.nih.gov books NBK1173 GeneReviews NCBI NIH UW entry on Mitochondrial DNA Associated Leigh Syndrome and NARP Mitochondrial enzymes genetics stub ... more details
Nuclear DNA , nuclear deoxyribonucleic acid nDNA , is DNA contained within a cell nucleus nucleus of eukaryote eukaryotic organisms . ref http medical dictionary.thefreedictionary.com DNADNA definition in the Medical dictionary ref In mammals and vertebrate s, nuclear DNA encodes more of the genome than the mitochondrialDNA and is composed of information inherited from two parents, one male, and one female, rather than matrilineally . ref http en.mimi.hu biology nuclear genome.html Nuclear genome ref Nuclear DNA is the most common DNA used in forensic examinations. ref http www.fbi.gov about us lab dna nuclear FBI Laboratory Services Nuclear DNA Unit ref References reflist See also Nuclear gene Chromatin Nucleic acids DEFAULTSORT Nuclear Dna Category DNA Cell biology stub ar ca ADN nuclear fr ADN nucl aire pl NDNA pt DNA nuclear ... more details
orphan date September 2010 It is a DNA contained in organelle s, outside the cell nucleus nucleus of eukaryote Eukaryotic cells . Examples mitochondria contain mitochondrialDNA plastid s e.g., chloroplasts contain plastid DNA Structure Unlike nuclear DNA , which is present as linear molecule s inside the chromosome s, organellar DNA is present as circular molecules of high copy number. Also, because organelles are uniparentally inherited in many organisms, so is their organellar DNA. See also Nuclear DNA Category DNA biology stub ar ... more details
refimprove date June 2010 Infobox Disease Name PAGENAME Image Caption DiseasesDB 32948 ICD10 ICD9 ICD9 277.87 ICDO OMIM 603041 MedlinePlus eMedicineSubj eMedicineTopic MeshID Mitochondrial neurogastrointestinal encephalopathy syndrome MNGIE , also called myoneurogastrointestinal encephalopathy syndrome or POLIP syndrome , ref name omim OMIM 603041 ref is a rare autosome autosomal dominance genetics recessive ref name mnear cite pmid 19056268 ref mitochondrial disease usually appearing between the second and fifth decades of life. Unlike typical mitochondrial diseases caused by mitochondrial DNA mtDNA mutations, MNGIE is caused by mutations in the ECGF1 TYMP gene, which encodes the enzyme thymidine phosphorylase. ref name omim A secondary form of MNGIE, called MNGIE without leukoencephalopathy , can be caused by mutations in the POLG gene. ref name omim Signs and symptoms MNGIE is a multisystem disorder. Gastrointestinal symptoms may include gastrointestinal dysmotility possibly resulting in pseudo obstruction in which the muscular contractions peristalsis of the gastrointestinal tract become inefficient causing malabsorption . Borborygmi stomach rumbling , early satiety, diarrhea, constipation, gastroparesis , nausea, vomiting, weight loss, diverticulitis . Neurological symptoms may include diffuse leukoencephalopathy , peripheral neuropathy , and myopathy .Ocular symptoms may include retinal degeneration, ophthalmoplegia paralysis of eye muscles , ptosis drooping eyelids . Those with MNGIE are often thin, experiencing continuous weight loss. References reflist External links http www.ncbi.nlm.nih.gov bookshelf br.fcgi?book gene&part mngie GeneReview NIH UW entry on Mitochondrial Neurogastrointestinal Encephalopathy Disease Mitochondrial diseases Inborn errors of purine pyrimidine metabolism DEFAULTSORT Mitochondrial Neurogastrointestinal Encephalopathy Syndrome Category Mitochondrial diseases Category Rare diseases Category Syndromes Category Autosomal recessive di ... more details
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