Dev109496 1418..1430

نویسندگان

  • Jeffrey M. Alexander
  • Swetansu K. Hota
  • Daniel He
  • Sean Thomas
  • Lena Ho
  • Len A. Pennacchio
  • Benoit G. Bruneau
چکیده

The interplay between different levels of gene regulation in modulating developmental transcriptional programs, such as histonemodifications and chromatin remodeling, is not well understood. Here, we show that the chromatin remodeling factor Brg1 is required for enhancer activation in mesoderm induction. In an embryonic stem cell-based directed differentiation assay, the absence of Brg1 results in a failure of cardiomyocyte differentiation and broad deregulation of lineagespecific geneexpressionduringmesoderm induction.We find thatBrg1 co-localizeswithH3K27acat distal enhancers and is required for robust H3K27 acetylation at distal enhancers that are activated during mesoderm induction. Brg1 is also required to maintain Polycombmediated repression of non-mesodermal developmental regulators, suggesting cooperativity between Brg1 and Polycomb complexes. Thus, Brg1 is essential for modulating active and repressive chromatin states during mesoderm lineage commitment, in particular the activation of developmentally important enhancers. These findings demonstrate interplay between chromatin remodeling complexes and histone modifications that, together, ensure robust and broad gene regulation during crucial lineage commitment decisions.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

0(1430)ll decay within QCD sum rules

Form factors of rare B → K 0 (1430)l+l− decay are calculated within three–point QCD sum rules, with K 0 (1430) being the p–wave scalar meson. The branching ratios are estimated when only short, as well as short and long distance effects, are taken into account. It is obtained that the B → K 0 (1430)l+l− (l = e, μ) decay is measurable at LHC. Measurement of these branching ratios for the semilep...

متن کامل

Drugs 2007; 67 (10): 1411-1427

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1412 1. Respiratory Syncytial Virus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1413 1.1 Epidemiology . . . . . . . . . . . . . . . . . . . . . . . ....

متن کامل

Analysis of B → K ∗ 0 ( 1430 ) l + l − Decay in the Supersymmetric Models

In this paper, we study the branching ratios of B → K 0 (1430)l+l− decay, where K 0 (1430) being the p–wave scalar meson, in the supersymmetric models. The branching ratios are estimated when short and long distance effects are taken into account. It is found that the B → K 0 (1430)l+l− (l = μ, τ) decay is measurable at LHC. Measurement of these branching ratios for the semileptonic rare B → K ...

متن کامل

0 ( 1430 ) l + l − decays in the Supersymmetric Models

In this paper, we compare the branching ratio and rate difference of electron channel to muon channel of B → K 0 (1430)l+l− and B → K∗l+l−decays, where K 0 (1430) is the p–wave scalar meson, in the supersymmetric models. MSSM with R parity is considered since considerable deviation from the standard model predictions can be obtained in B → Xsll. Taking CQ1 and CQ2 about one which is consistent ...

متن کامل

Pii: S0003-4878(00)00077-6

†Department of Environmental Health, School of Public Health and Tropical Medicine, Tulane University Medical Center, 1430 Tulane Avenue, New Orleans, LA 70112 USA; ‡Department of Biostatistics, School of Public Health and Tropical Medicine, Tulane University Medical Center, 1430 Tulane Avenue, New Orleans, LA 70112 USA; §Department of Medicine, School of Medicine, Tulane University Medical Cen...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2015