Suppr超能文献

10条人类染色体的5个核苷酸分辨率转录图谱。

Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution.

作者信息

Cheng Jill, Kapranov Philipp, Drenkow Jorg, Dike Sujit, Brubaker Shane, Patel Sandeep, Long Jeffrey, Stern David, Tammana Hari, Helt Gregg, Sementchenko Victor, Piccolboni Antonio, Bekiranov Stefan, Bailey Dione K, Ganesh Madhavan, Ghosh Srinka, Bell Ian, Gerhard Daniela S, Gingeras Thomas R

机构信息

Affymetrix Inc., Santa Clara, CA 95051, USA.

出版信息

Science. 2005 May 20;308(5725):1149-54. doi: 10.1126/science.1108625. Epub 2005 Mar 24.

Abstract

Sites of transcription of polyadenylated and nonpolyadenylated RNAs for 10 human chromosomes were mapped at 5-base pair resolution in eight cell lines. Unannotated, nonpolyadenylated transcripts comprise the major proportion of the transcriptional output of the human genome. Of all transcribed sequences, 19.4, 43.7, and 36.9% were observed to be polyadenylated, nonpolyadenylated, and bimorphic, respectively. Half of all transcribed sequences are found only in the nucleus and for the most part are unannotated. Overall, the transcribed portions of the human genome are predominantly composed of interlaced networks of both poly A+ and poly A- annotated transcripts and unannotated transcripts of unknown function. This organization has important implications for interpreting genotype-phenotype associations, regulation of gene expression, and the definition of a gene.

摘要

在8种细胞系中,以5个碱基对的分辨率绘制了10条人类染色体的多聚腺苷酸化和非多聚腺苷酸化RNA的转录位点图谱。未注释的非多聚腺苷酸化转录本占人类基因组转录输出的主要部分。在所有转录序列中,分别观察到19.4%、43.7%和36.9%为多聚腺苷酸化、非多聚腺苷酸化和双态的。所有转录序列的一半仅在细胞核中发现,并且大部分未注释。总体而言,人类基因组的转录部分主要由多聚A+和多聚A-注释转录本以及功能未知的未注释转录本的交错网络组成。这种组织形式对于解释基因型-表型关联、基因表达调控和基因定义具有重要意义。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验