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完成人类基因组的常染色质序列测定。

Finishing the euchromatic sequence of the human genome.

出版信息

Nature. 2004 Oct 21;431(7011):931-45. doi: 10.1038/nature03001.

Abstract

The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers approximately 99% of the euchromatic genome and is accurate to an error rate of approximately 1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human genome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead.

摘要

人类基因组序列编码了人类生理机能的遗传指令,以及有关人类进化的丰富信息。2001年,国际人类基因组测序联盟公布了人类基因组常染色质部分的序列草图。从那时起,国际合作一直在努力将该草图转化为一个高精度且覆盖率近乎完整的基因组序列。在此,我们报告这一完成过程的结果。当前的基因组序列(构建版本35)包含28.5亿个核苷酸,仅有341个间隙。它覆盖了约99%的常染色质基因组,错误率约为每10万个碱基发生1次错误。许多剩余的常染色质间隙与节段性重复有关,需要采用新方法进行重点研究。这个近乎完整的序列是脊椎动物的首个此类序列,极大地提高了对人类基因组进行生物学分析的精度,包括对基因数量、产生和消亡的研究。值得注意的是,人类基因组似乎仅编码2万至2.5万个蛋白质编码基因。本文报道的基因组序列应成为未来几十年生物医学研究的坚实基础。

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