词条 | MSRA (gene) |
释义 |
FunctionMsr is ubiquitous and highly conserved. Human and animal studies have shown the highest levels of expression in kidney and liver. It carries out the enzymatic reduction of methionine sulfoxide (MetO), the oxidized form of the amino acid methionine (Met), back to methionine, using thioredoxin to catalyze the enzymatic reduction and repair of oxidized methionine residues.[3] Its proposed function is thus the repair of oxidative damage to proteins to restore biological activity.[2] Oxidation of methionine residues in tissue proteins can cause them to misfold or otherwise render them dysfunctional.[3] Clinical significanceMetO increases with age in body tissues, which is believed by some to contribute to biological ageing.[3][4] Moreover, levels of methionine sulfoxide reductase A (MsrA) decline in aging tissues in mice and in association with age-related disease in humans.[3] There is thus a rationale for thinking that by maintaining the structureincreased levels or activity of MsrA might retard the rate of aging. Indeed, transgenic Drosophila (fruit flies) that overexpress methionine sulfoxide reductase show extended lifespan.[5] However, the effects of MsrA overexpression in mice were ambiguous.[6] MsrA is found in both the cytosol and the energy-producing mitochondria, where most of the body's endogenous free radicals are produced. Transgenically increasing the levels of MsrA in either the cytosol or the mitochondria had no significant effect on lifespan assessed by most standard statistical tests, and may possibly have led to early deaths in the cytosol-specific mice, although the survival curves appeared to suggest a slight increase in maximum (90%) survivorship, as did analysis using Boschloo's Exact test, a binomial test designed to test greater extreme variation.[6] Deletion of this gene has been associated with insulin resistance in mice,[7] while overexpression reduces insulin resistance in old mice.[6] See also
References1. ^{{cite journal |vauthors=Kuschel L, Hansel A, Schonherr R, Weissbach H, Brot N, Hoshi T, Heinemann SH | title = Molecular cloning and functional expression of a human peptide methionine sulfoxide reductase (hMsrA) | journal = FEBS Lett | volume = 456 | issue = 1 | pages = 17–21 |date=Sep 1999 | pmid = 10452521 | pmc = | doi =10.1016/S0014-5793(99)00917-5 }} 2. ^1 {{cite web | title = Entrez Gene: MSRA methionine sulfoxide reductase A| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4482| accessdate = }} 3. ^1 2 3 {{cite journal |vauthors=Stadtman ER, Van Remmen H, Richardson A, Wehr NB, Levine RL | title=Methionine oxidation and aging | journal=Biochimica et Biophysica Acta | volume=1703 | issue=2 | year=2005 | pages=135–140 | pmid=15680221 | doi=10.1016/j.bbapap.2004.08.010}} 4. ^{{cite journal |vauthors=Shringarpure R, Davies KJ | title=Protein turnover by the proteasome in aging and disease | journal=Free Radical Biology & Medicine | volume=32 | issue=11 | year=2002 | pages=1084–1089 | pmid=12031893 | doi=10.1016/S0891-5849(02)00824-9}} 5. ^{{cite journal |vauthors=Ruan H, Tang XD, Chen ML, Joiner ML, Sun G, Brot N, Weissbach H, Heinemann SH, Iverson L, Wu CF, Hoshi T | title=High-quality life extension by the enzyme peptide methionine sulfoxide reductase | journal=Proceedings of the National Academy of Sciences of the United States of America | volume=99 | issue=5 | year=2002 | pages=2748–2753 | url = http://www.pnas.org/content/99/5/2748.full| id= | pmid=11867705 | doi=10.1073/pnas.032671199 | pmc=122419}} 6. ^1 2 {{cite journal|vauthors=Salmon AB, Kim G, Liu C, Wren JD, Georgescu C, Richardson A, Levine RL|title=Effects of transgenic methionine sulfoxide reductase A (MsrA) expression on lifespan and age-dependent changes in metabolic function in mice|journal=Redox Biol|date=December 2016|volume=10|pages=251–256|doi=10.1016/j.redox.2016.10.012|pmid=27821326|url=http://www.sciencedirect.com/science/article/pii/S2213231716301987|accessdate=21 November 2016|pmc=5099276}} 7. ^{{cite journal |vauthors=Styskal JL, Nwagwu FA, Watkins YN, Liang H, Richardson A, Musi N, Salmon AB | title = Methionine sulfoxide reductase a affects insulin resistance by protecting insulin receptor function | journal = Free Radic. Biol. Med. | volume = 56| issue = | pages = 123–32|date=October 2012 | pmid = 23089224 | doi = 10.1016/j.freeradbiomed.2012.10.544 | pmc = 3578155}} Further reading{{refbegin | 2}}
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