人类特异性神经SRGAP2基因的演变通过不完整的细分重复
Megan Y Dennis1, Xander Nuttle, Peter H Sudmant
1Department of Genome Sciences, University of Washington School of Medicine, Seattle, 98195, USA.
Cell
|May 8, 2012
概括
人类特异性的SRGAP2基因重复发生了三次,导致一种新的功能,这可能是人类进化过程中驱动新皮质扩张的原因.
科学领域:
- 遗传学 是一个遗传学.
- 进化生物学 进化生物学
- 人类起源的人类起源
背景情况:
- 基因重复是进化创新和表型多样性的关键驱动力.
- 裂纹-Robo Rho GTPase激活蛋白2 (SRGAP2) 基因在皮层发育中起作用.
研究的目的:
- 识别和描述人类特异性的基因重复.
- 调查SRGAP2重复的进化史和功能影响.
主要方法:
- 利用一个平分体水分形分子来识别缺失的序列.
- 基因组比较分析到目前为止的重复事件.
- 复制基因的序列和表达分析.
主要成果:
- 在人类血统中,SRGAP2基因复制了三次.
- 复制事件发生在大约3.4,2.4和100万年前.
- SRGAP2C是最可能的功能重复,可能会对抗父母的SRGAP2功能.
结论:
- SRGAP2重复代表了一种在人类进化早期出现的新型基因功能.
- 这些重复与过渡到Homo属和新皮层扩张相吻合.
- SRGAP2C的出现可能对人类认知进化至关重要.
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