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   Evidence for positive selection on a number of microRNA regulatory interactions during recent human evolution  
   
نویسنده li j. ,liu y. ,xin x. ,kim t.s. ,cabeza e.a. ,ren j. ,nielsen r. ,wrana j.l. ,zhang z.
منبع plos genetics - 2012 - دوره : 8 - شماره : 3
چکیده    Microrna (mirna)-mediated gene regulation is of critical functional importance in animals and is thought to be largely constrained during evolution. however,little is known regarding evolutionary changes of the mirna network and their role in human evolution. here we show that a number of mirna binding sites display high levels of population differentiation in humans and thus are likely targets of local adaptation. in a subset we demonstrate that allelic differences modulate mirna regulation in mammalian cells,including an interaction between mir-155 and tyrp1,an important melanosomal enzyme associated with human pigmentary differences. we identify alternate alleles of tyrp1 that induce or disrupt mir-155 regulation and demonstrate that these alleles are selected with different modes among human populations,causing a strong negative correlation between the frequency of mir-155 regulation of tyrp1 in human populations and their latitude of residence. we propose that local adaptation of microrna regulation acts as a rheostat to optimize tyrp1 expression in response to differential uv radiation. our findings illustrate the evolutionary plasticity of the microrna regulatory network in recent human evolution. © 2012 li et al. this is an open-access article distributed under the terms of the creative commons attribution license,which permits unrestricted use,distribution,and reproduction in any medium,provided the original author and source are credited.
آدرس banting and best department of medical research,the donnelly centre,university of toronto,toronto,canada,department of molecular genetics,university of toronto,toronto,canada,department of genetics,stanford university school of medicine,stanford,ca, United States, department of molecular genetics,university of toronto,toronto,canada,the center for systems biology,samuel lunenfeld research institute,mount sinai hospital,toronto, Canada, banting and best department of medical research,the donnelly centre,university of toronto,toronto,canada,department of molecular genetics,university of toronto,toronto,canada,department of biological engineering,massachusetts institute of technology,cambridge,ma, United States, banting and best department of medical research,the donnelly centre,university of toronto,toronto, Canada, the center for systems biology,samuel lunenfeld research institute,mount sinai hospital,toronto, Canada, department of physics and centre for computational science and engineering,national university of singapore,singapore, Singapore, departments of integrative biology and statistics,university of california berkeley,berkeley,ca, United States, department of molecular genetics,university of toronto,toronto,canada,the center for systems biology,samuel lunenfeld research institute,mount sinai hospital,toronto, Canada, banting and best department of medical research,the donnelly centre,university of toronto,toronto,canada,department of molecular genetics,university of toronto,toronto, Canada
 
     
   
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