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人类21号染色体的近着丝粒区域富含假基因和基因片段。

Juxta-centromeric region of human chromosome 21 is enriched for pseudogenes and gene fragments.

作者信息

Ruault M, Trichet V, Gimenez S, Boyle S, Gardiner K, Rolland M, Roizès G, De Sario A

机构信息

Séquences Répétées et Centromères Humains, CNRS UPR 1142, Institut de Biologie, Montpellier, France.

出版信息

Gene. 1999 Oct 18;239(1):55-64. doi: 10.1016/s0378-1119(99)00381-9.

Abstract

A physical map including four pseudogenes and 10 gene fragments and spanning 500 kb in the juxta-centromeric region of the long arm of human chromosome 21 is presented. cDNA fragments isolated from a selected cDNA library were characterized and mapped to the 831B6 YAC and to two BAC contigs that cover 250 kb of the region. An 85 kb genomic sequence located in the proximal region of the map was analyzed for putative exons. Four pseudogenes were found, including psiIGSF3, psiEIF3, psiGCT-rel whose functional copies map to chromosome 1p13, chromosome 2 and chromosome 22q11, respectively. The TTLL1 pseudogene corresponds to a new gene whose functional copy maps to chromosome 22q13. Ten gene fragments represent novel sequences that have related sequences on different human chromosomes and show 97-100% nucleotide identity to chromosome 21. These may correspond to pseudogenes on chromosome 21 and to functional genes in other chromosomes. The 85 kb genomic sequence was analyzed also for GC content, CpG islands, and repetitive sequence distribution. A GC-poor L isochore spanning 40 kb from satellite 1 was observed in the most centromeric region, next to a GC-rich H isochore that is a candidate region for the presence of functional genes. The pericentric duplication of a 7.8 kb region that is derived from the 22q13 chromosome band is described. We showed that the juxta-centromeric region of human chromosome 21 is enriched for retrotransposed pseudogenes and gene fragments transferred by interchromosome duplications, but we do not rule out the possibility that the region harbors functional genes also.

摘要

本文展示了一张物理图谱,该图谱涵盖人类21号染色体长臂近着丝粒区域的4个假基因和10个基因片段,跨度为500 kb。从选定的cDNA文库中分离出的cDNA片段进行了特征分析,并定位到831B6 YAC以及覆盖该区域250 kb的两个BAC重叠群上。对位于图谱近端区域的一个85 kb基因组序列进行了推定外显子分析。发现了4个假基因,包括psiIGSF3、psiEIF3、psiGCT-rel,其功能拷贝分别定位于1号染色体p13区域、2号染色体和22号染色体q11区域。TTLL1假基因对应一个新基因,其功能拷贝定位于22号染色体q13区域。10个基因片段代表了新的序列,这些序列在不同人类染色体上有相关序列,与21号染色体的核苷酸同一性为97 - 100%。这些可能对应于21号染色体上的假基因以及其他染色体上的功能基因。还对85 kb基因组序列的GC含量、CpG岛和重复序列分布进行了分析。在最靠近着丝粒的区域观察到一个从卫星1开始跨度为40 kb的GC含量低的L等臂染色质,旁边是一个GC含量高的H等臂染色质,该区域是功能基因存在的候选区域。描述了一个源自22号染色体q13带的7.8 kb区域的着丝粒周围重复。我们表明,人类21号染色体的近着丝粒区域富含逆转座假基因和通过染色体间重复转移的基因片段,但我们不排除该区域也含有功能基因的可能性。

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