人类加速区域1
Human Accelerated Region 1

原始链接: https://en.wikipedia.org/wiki/Human_accelerated_region_1

## 人类加速区域1 (HAR1): 摘要 人类加速区域1 (HAR1) 是人类染色体20上一个独特的DNA片段,与其他哺乳动物相比,表现出显著的进化差异。HAR1被认为是人类基因组中进化最快的区域之一,包含两个非编码RNA基因,HAR1A和HAR1B。 HAR1A尤其值得注意的是,它在关键的大脑发育阶段表达——妊娠的第7到18周之间——特别是在发育中的皮层以及后来的小脑和前脑中。其RNA结构异常稳定,并且与黑猩猩不同,表明它在人类特有的脑部进化中发挥功能作用。 研究表明HAR1A与reelin蛋白相互作用,reelin蛋白对神经元迁移很重要。此外,在亨廷顿舞蹈症患者中,其表达受到抑制,可能导致神经退化。HAR1B在染色体上与HAR1A重叠,但在大脑中的表达水平较低。总而言之,HAR1代表了一个迷人的例子,展示了基因组变化与人类特有的神经系统发育之间的联系。

黑客新闻 新 | 过去 | 评论 | 提问 | 展示 | 招聘 | 提交 登录 人类加速区域 1 (wikipedia.org) 11 分,apollinaire 发表于 2 小时前 | 隐藏 | 过去 | 收藏 | 讨论 帮助 指南 | 常见问题 | 列表 | API | 安全 | 法律 | 申请 YC | 联系 搜索:
相关文章

原文

From Wikipedia, the free encyclopedia

Segment of chromosome 20 in humans

RNA family

In molecular biology, Human Accelerated Region 1 (Highly Accelerated Region 1, HAR1) is a segment of the human genome found on the long arm of chromosome 20. It is a human accelerated region. It is located within a pair of overlapping long non-coding RNA genes, HAR1A (HAR1F) and HAR1B (HAR1R).[1]

HAR1A is expressed in Cajal–Retzius cells, contemporaneously with the protein reelin.[1][2][3]

HAR1A was identified in August 2006 when human accelerated regions (HARs) were first investigated. These 49 regions represent parts of the human genome that differ significantly from highly conserved regions of our closest ancestors in terms of evolution. Many of the HARs are associated with genes known to play a role in neurodevelopment. One particularly altered region, HAR1, was found in a stretch of genome with no known protein-coding RNA sequences. Two RNA genes, HAR1F and HAR1R, were identified partly within the region. The RNA structure of HAR1A has been shown to be stable, with a secondary structure unlike those previously described.

HAR1A is active in the developing human brain between the 7th and 18th gestational weeks. It is found in the dorsal telencephalon in fetuses. In adult humans, it is found throughout the cerebellum and forebrain; it is also found in the testes.[1] There is evidence that HAR1 is repressed by REST in individuals with Huntington's disease, perhaps contributing to the neurodegeneration associated with the disease.[4]

Further work on the secondary structure of HAR1A has suggested that the human form adopts a different fold to that of other mammals exemplified by the chimpanzee sequence.[5]

The HAR1B gene overlaps HAR1A, and is located on the opposite strand of the chromosome. Its expression in the human brain is lower than that of HAR1A.[1]

  1. ^ a b c d Pollard KS, Salama SR, Lambert N, Lambot MA, Coppens S, Pedersen JS, Katzman S, King B, Onodera C, Siepel A, Kern AD, Dehay C, Igel H, Ares M Jr, Vanderhaeghen P, Haussler D (2006-08-16). "An RNA gene expressed during cortical development evolved rapidly in humans" (PDF). Nature. 443 (7108): 167–172. Bibcode:2006Natur.443..167P. doi:10.1038/nature05113. hdl:2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51805. PMID 16915236. S2CID 18107797. supplement
  2. ^ Pollard KS, Salama SR, King B, et al. (October 2006). "Forces shaping the fastest evolving regions in the human genome". PLOS Genet. 2 (10): e168. doi:10.1371/journal.pgen.0020168. PMC 1599772. PMID 17040131.
  3. ^ Amadio JP, Walsh CA (September 2006). "Brain evolution and uniqueness in the human genome". Cell. 126 (6): 1033–1035. doi:10.1016/j.cell.2006.09.007. PMID 16990130. S2CID 16034905.
  4. ^ Johnson R, Richter N, Jauch R, Gaughwin PM, Zuccato C, Cattaneo E, Stanton LW (2010). "The Human Accelerated Region 1 noncoding RNA is repressed by REST in Huntington's disease". Physiol Genomics. 41 (3): 269–274. doi:10.1152/physiolgenomics.00019.2010. PMID 20179156. S2CID 25653037.
  5. ^ Beniaminov A, Westhof E, Krol A (July 2008). "Distinctive structures between chimpanzee and human in a brain noncoding RNA". RNA. 14 (7): 1270–1275. doi:10.1261/rna.1054608. PMC 2441984. PMID 18511501.
联系我们 contact @ memedata.com