Temporal dynamics and genetic control of transcription in the human prefrontal cortex

被引:530
|
作者
Colantuoni, Carlo [1 ,2 ,3 ,4 ]
Lipska, Barbara K. [1 ]
Ye, Tianzhang [1 ]
Hyde, Thomas M. [1 ,4 ]
Tao, Ran [1 ]
Leek, Jeffrey T. [2 ]
Colantuoni, Elizabeth A. [2 ]
Elkahloun, Abdel G. [5 ]
Herman, Mary M. [1 ]
Weinberger, Daniel R. [1 ,4 ]
Kleinman, Joel E. [1 ]
机构
[1] NIMH, Sect Neuropathol, Clin Brain Disorders Branch, Genes Cognit & Psychosis Program,IRP,NIH, Bethesda, MD 20892 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD 21205 USA
[3] Illuminato Biotechnol Inc, Baltimore, MD 21211 USA
[4] Johns Hopkins Univ, Med Ctr, Lieber Inst Brain Dev, Baltimore, MD 21205 USA
[5] NHGRI, Canc Genet Branch, NIH, Bethesda, MD 20892 USA
关键词
HUMAN BRAIN; EXPRESSION; DISEASE; MOUSE; MICRORNA; RNA;
D O I
10.1038/nature10524
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Previous investigations have combined transcriptional and genetic analyses in human cell lines(1-3), but few have applied these techniques to human neural tissue(4-8). To gain a global molecular perspective on the role of the human genome in cortical development, function and ageing, we explore the temporal dynamics and genetic control of transcription in human prefrontal cortex in an extensive series of post-mortem brains from fetal development through ageing. We discover a wave of gene expression changes occurring during fetal development which are reversed in early postnatal life. One half-century later in life, this pattern of reversals is mirrored in ageing and in neurodegeneration. Although we identify thousands of robust associations of individual genetic polymorphisms with gene expression, we also demonstrate that there is no association between the total extent of genetic differences between subjects and the global similarity of their transcriptional profiles. Hence, the human genome produces a consistent molecular architecture in the prefrontal cortex, despite millions of genetic differences across individuals and races. To enable further discovery, this entire data set is freely available (from Gene Expression Omnibus: accession GSE30272; and dbGaP: accession phs000417.v1.p1) and can also be interrogated via a biologist-friendly stand-alone application (http://www.libd.org/braincloud).
引用
收藏
页码:519 / U117
页数:6
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