胎盘特异性IGF-II是胎盘和胎儿生长的主要调节剂
Miguel Constância1, Myriam Hemberger, Jennifer Hughes
1Laboratory of Developmental Genetics and Imprinting, Developmental Genetics Programme, The Babraham Institute, Cambridge CB2 4AT, UK. miguel.constancia@bbsrc.ac.uk
Nature
|June 28, 2002
概括
从Igf2基因中删除P0转录会损害胎盘营养物质的运输,导致胎儿生长受到限制. 这突显了印制基因在调节胎儿营养供应中的作用.
科学领域:
- 遗传学 是一个遗传学.
- 发展生物学 发展生物学
- 生殖生物学 生殖生物学
背景情况:
- 印制基因对于哺乳动物的胎盘发育和胎儿生长至关重要,其表达仅限于一个父母染色体.
- 胰岛素样生长因子II (Igf2) 基因在胎儿和胎盘中都受到父亲的表达.
研究的目的:
- 调查Igf2基因中的P0转录的作用,具体表达在胎盘迷宫热囊细胞中.
- 确定P0转录删除对胎盘功能和胎儿发育的影响.
主要方法:
- 在哺乳动物模型中,从Igf2基因中删除P0转录的基因.
- 对胎盘生长,胎儿生长和营养物质运输机制 (被动透性和活性氨基酸运输) 的分析.
主要成果:
- 删除P0转录导致胎盘生长减少,随后胎儿生长受限.
- 突变的胎盘显示了被动营养透性下降,最初由高调节的活性氨基酸运输补偿.
- 随着时间的推移,这种补偿失败了,导致持续的胎儿生长限制和胎儿与胎盘体重比率的增加.
结论:
- 印制基因作用,特别是Igf2的P0转录,通过胎盘功能直接控制母亲向胎儿提供营养.
- 这些发现支持印记的遗传冲突理论,表明Igf2既能调节胎盘营养供应,也能调节胎儿营养需求.
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