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   Developmental Programming Mediated by Complementary Roles of Imprinted Grb10 in Mother and Pup  
   
نویسنده cowley m. ,garfield a.s. ,madon-simon m. ,charalambous m. ,clarkson r.w. ,smalley m.j. ,kendrick h. ,isles a.r. ,parry a.j. ,carney s. ,oakey r.j. ,heisler l.k. ,moorwood k. ,wolf j.b. ,ward a.
منبع plos biology - 2014 - دوره : 12 - شماره : 2
چکیده    Developmental programming links growth in early life with health status in adulthood. although environmental factors such as maternal diet can influence the growth and adult health status of offspring,the genetic influences on this process are poorly understood. using the mouse as a model,we identify the imprinted gene grb10 as a mediator of nutrient supply and demand in the postnatal period. the combined actions of grb10 expressed in the mother,controlling supply,and grb10 expressed in the offspring,controlling demand,jointly regulate offspring growth. furthermore,grb10 determines the proportions of lean and fat tissue during development,thereby influencing energy homeostasis in the adult. most strikingly,we show that the development of normal lean/fat proportions depends on the combined effects of grb10 expressed in the mother,which has the greater effect on offspring adiposity,and grb10 expressed in the offspring,which influences lean mass. these distinct functions of grb10 in mother and pup act complementarily,which is consistent with a coadaptation model of imprinting evolution,a model predicted but for which there is limited experimental evidence. in addition,our findings identify grb10 as a key genetic component of developmental programming,and highlight the need for a better understanding of mother-offspring interactions at the genetic level in predicting adult disease risk. © 2014 cowley et al.
آدرس department of biology and biochemistry and centre for regenerative medicine,university of bath,bath,united kingdom,department of medical and molecular genetics,king's college london,london, United Kingdom, department of biology and biochemistry and centre for regenerative medicine,university of bath,bath,united kingdom,department of pharmacology,university of cambridge,cambridge, United Kingdom, department of biology and biochemistry and centre for regenerative medicine,university of bath,bath,united kingdom,department of cell biology,university of geneva,geneva, Switzerland, department of physiology,development and neuroscience,university of cambridge,cambridge,united kingdom,centre for endocrinology,william harvey research institute,barts and the london school of medicine and dentistry,queen mary university of london,london, United Kingdom, cardiff school of biosciences,cardiff university,cardiff, United Kingdom, european cancer stem cell research institute,cardiff school of biosciences,biomedical sciences building,cardiff university,cardiff, United Kingdom, european cancer stem cell research institute,cardiff school of biosciences,biomedical sciences building,cardiff university,cardiff, United Kingdom, behavioural genetics group,mrc centre for neuropsychiatric genetics and genomics,neuroscience and mental health research institute,schools of medicine and psychology,cardiff university,cardiff, United Kingdom, department of biology and biochemistry and centre for regenerative medicine,university of bath,bath, United Kingdom, department of biology and biochemistry and centre for regenerative medicine,university of bath,bath, United Kingdom, department of medical and molecular genetics,king's college london,london, United Kingdom, department of pharmacology,university of cambridge,cambridge, United Kingdom, department of biology and biochemistry and centre for regenerative medicine,university of bath,bath, United Kingdom, department of biology and biochemistry and centre for regenerative medicine,university of bath,bath, United Kingdom, department of biology and biochemistry and centre for regenerative medicine,university of bath,bath, United Kingdom
 
     
   
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