Using reporter gene assays to identify cis regulatory differences between humans and chimpanzees

被引:17
作者
Chabot, Adrien [1 ]
Shrit, Ralla A. [1 ]
Blekhman, Ran [1 ]
Gilad, Yoav [1 ]
机构
[1] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
关键词
D O I
10.1534/genetics.107.073429
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Most phenotypic differences between human and chimpanzee are likely to result from differences in gene regulation, rather than changes to protein-coding regions. To date, however, only a handful of human-chimpanzee nucleotide differences leading to changes in gene regulation have been identified. To hone in on differences in regulatory elements between human and chimpanzee, we focused on 10 genes that were previously found to be differentially expressed between the two species. We then designed reporter gene assays for the putative human and chimpanzee promoters of the 10 genes. Of seven promoters that we found to be active in human liver cell lines, human and chimpanzee promoters had significantly different activity in four cases, three of which recapitulated the gene expression difference seen in the microarray experiment. For these three genes, we were therefore able to demonstrate that a change in cis influences expression differences between humans and chimpanzees. Moreover, using site-directed mutagenesis on one construct, the promoter for the DDA3 gene, we were able to identify three nucleotides that together lead to a cis regulatory difference between the species. High-throughput application of this approach can provide a map of regulatory element differences between humans and our close evolutionary relatives.
引用
收藏
页码:2069 / 2076
页数:8
相关论文
共 54 条
[1]   Bmp4 and morphological variation of beaks in Darwin's finches [J].
Abzhanov, A ;
Protas, M ;
Grant, BR ;
Grant, PR ;
Tabin, CJ .
SCIENCE, 2004, 305 (5689) :1462-1465
[2]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[3]   REPETITIVE AND NON-REPETITIVE DNA SEQUENCES AND A SPECULATION ON ORIGINS OF EVOLUTIONARY NOVELTY [J].
BRITTEN, RJ ;
DAVIDSON, EH .
QUARTERLY REVIEW OF BIOLOGY, 1971, 46 (02) :111-+
[4]   A high proportion of chromosome 21 promoter polymorphisms influence transcriptional activity [J].
Buckland, PR ;
Coleman, SL ;
Hoogendoorn, B ;
Guy, C ;
Smith, SK ;
O'Donovan, MC .
GENE EXPRESSION-THE JOURNAL OF LIVER RESEARCH, 2003, 11 (5-6) :233-239
[5]   A high proportion of polymorphisms in the promoters of brain expressed genes influences transcriptional activity [J].
Buckland, PR ;
Hoogendoom, B ;
Guy, CA ;
Coleman, SL ;
Smith, SK ;
Buxbaum, JD ;
Haroutunian, V ;
O'Donovan, MC .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2004, 1690 (03) :238-249
[6]   Genetics and the making of Homo sapiens [J].
Carroll, SB .
NATURE, 2003, 422 (6934) :849-857
[7]  
Carroll SB, 2004, DNA DIVERSITY MOL GE
[8]  
*CHIPM SEQ AN CONS, 2005, NATURE, V437, P69
[9]   A distant upstream enhancer at the maize domestication gene tb1 has pleiotropic effects on plant and inflorescent architecture [J].
Clark, RM ;
Wagler, TN ;
Quijada, P ;
Doebley, J .
NATURE GENETICS, 2006, 38 (05) :594-597
[10]   Comprehensive analysis of transcriptional promoter structure and function in 1% of the human genome [J].
Cooper, SJ ;
Trinklein, ND ;
Anton, ED ;
Nguyen, L ;
Myers, RM .
GENOME RESEARCH, 2006, 16 (01) :1-10