人类中心阵列在经历破裂诱导复制的细胞中的扩张
Soyeon Showman1,2,3, Paul B Talbert1,3, Yiling Xu1,3
1Basic Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
bioRxiv : the preprint server for biology
|November 28, 2023
概括
人类中间体数组通过体细胞内的膨胀和收缩迅速改变长度. 这种进化是由同源的重组蛋白RAD52和PIF1促进的,这表明断裂诱导的复制驱动着中间体序列的改变.
科学领域:
- 遗传学 是一个遗传学.
- 分子生物学分子生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
背景情况:
- 人类的中间体存在于α-卫星DNA数组中,它们表现出快速的进化和个体长度变化.
- 诸如不平等交叉和基因转换之类的机制被提议用于中心层数组长度变化.
- 中心层数组复杂组织的分子基础在实验上仍未得到验证.
结论:
- 中心层阵列长度在体细胞分裂过程中受到动态调节.
- 断裂诱导的复制是一种可能的驱动中心分子序列进化的机制.
- RAD52和PIF1在中心基DNA的快速演变中起着至关重要的作用.
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