Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcription.


Autoria(s): Kilpinen H.; Waszak S.M.; Gschwind A.R.; Raghav S.K.; Witwicki R.M.; Orioli A.; Migliavacca E.; Wiederkehr M.; Gutierrez-Arcelus M.; Panousis N.I.; Yurovsky A.; Lappalainen T.; Romano-Palumbo L.; Planchon A.; Bielser D.; Bryois J.; Padioleau I.; Udin G.; Thurnheer S.; Hacker D.; Core L.J.; Lis J.T.; Hernandez N.; Reymond A.; Deplancke B.; Dermitzakis E.T.
Data(s)

2013

Resumo

DNA sequence variation has been associated with quantitative changes in molecular phenotypes such as gene expression, but its impact on chromatin states is poorly characterized. To understand the interplay between chromatin and genetic control of gene regulation, we quantified allelic variability in transcription factor binding, histone modifications, and gene expression within humans. We found abundant allelic specificity in chromatin and extensive local, short-range, and long-range allelic coordination among the studied molecular phenotypes. We observed genetic influence on most of these phenotypes, with histone modifications exhibiting strong context-dependent behavior. Our results implicate transcription factors as primary mediators of sequence-specific regulation of gene expression programs, with histone modifications frequently reflecting the primary regulatory event.

Identificador

http://serval.unil.ch/?id=serval:BIB_3B38B04B8D47

isbn:1095-9203 (Electronic)

pmid:24136355

doi:10.1126/science.1242463

isiid:000326647600045

Idioma(s)

en

Fonte

Science, vol. 342, no. 6159, pp. 744-747

Tipo

info:eu-repo/semantics/article

article