USF1 and hSET1A mediated epigenetic modifications regulate lineage differentiation and HoxB4 transcription.

The interplay between polycomb and trithorax complexes has been implicated in embryonic stem cell (ESC) self-renewal and differentiation. It has been shown recently that WRD5 and Dpy-30, specific components of the SET1/MLL protein complexes, play important roles during ESC self-renewal and different...

Full description

Bibliographic Details
Main Authors: Changwang Deng, Ying Li, Shermi Liang, Kairong Cui, Tal Salz, Hui Yang, Zhanyun Tang, Patrick G Gallagher, Yi Qiu, Robert Roeder, Keji Zhao, Jörg Bungert, Suming Huang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-06-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3675019?pdf=render
_version_ 1818409600504823808
author Changwang Deng
Ying Li
Shermi Liang
Kairong Cui
Tal Salz
Hui Yang
Zhanyun Tang
Patrick G Gallagher
Yi Qiu
Robert Roeder
Keji Zhao
Jörg Bungert
Suming Huang
author_facet Changwang Deng
Ying Li
Shermi Liang
Kairong Cui
Tal Salz
Hui Yang
Zhanyun Tang
Patrick G Gallagher
Yi Qiu
Robert Roeder
Keji Zhao
Jörg Bungert
Suming Huang
author_sort Changwang Deng
collection DOAJ
description The interplay between polycomb and trithorax complexes has been implicated in embryonic stem cell (ESC) self-renewal and differentiation. It has been shown recently that WRD5 and Dpy-30, specific components of the SET1/MLL protein complexes, play important roles during ESC self-renewal and differentiation of neural lineages. However, not much is known about how and where specific trithorax complexes are targeted to genes involved in self-renewal or lineage-specification. Here, we report that the recruitment of the hSET1A histone H3K4 methyltransferase (HMT) complex by transcription factor USF1 is required for mesoderm specification and lineage differentiation. In undifferentiated ESCs, USF1 maintains hematopoietic stem/progenitor cell (HS/PC) associated bivalent chromatin domains and differentiation potential. Furthermore, USF1 directed recruitment of the hSET1A complex to the HoxB4 promoter governs the transcriptional activation of HoxB4 gene and regulates the formation of early hematopoietic cell populations. Disruption of USF or hSET1A function by overexpression of a dominant-negative AUSF1 mutant or by RNA-interference-mediated knockdown, respectively, led to reduced expression of mesoderm markers and inhibition of lineage differentiation. We show that USF1 and hSET1A together regulate H3K4me3 modifications and transcription preinitiation complex assembly at the hematopoietic-associated HoxB4 gene during differentiation. Finally, ectopic expression of USF1 in ESCs promotes mesoderm differentiation and enforces the endothelial-to-hematopoietic transition by inducing hematopoietic-associated transcription factors, HoxB4 and TAL1. Taken together, our findings reveal that the guided-recruitment of the hSET1A histone methyltransferase complex and its H3K4 methyltransferase activity by transcription regulator USF1 safeguards hematopoietic transcription programs and enhances mesoderm/hematopoietic differentiation.
first_indexed 2024-12-14T10:02:12Z
format Article
id doaj.art-7520ff3efccb466787cd50dec367ff8e
institution Directory Open Access Journal
issn 1553-7390
1553-7404
language English
last_indexed 2024-12-14T10:02:12Z
publishDate 2013-06-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Genetics
spelling doaj.art-7520ff3efccb466787cd50dec367ff8e2022-12-21T23:07:13ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042013-06-0196e100352410.1371/journal.pgen.1003524USF1 and hSET1A mediated epigenetic modifications regulate lineage differentiation and HoxB4 transcription.Changwang DengYing LiShermi LiangKairong CuiTal SalzHui YangZhanyun TangPatrick G GallagherYi QiuRobert RoederKeji ZhaoJörg BungertSuming HuangThe interplay between polycomb and trithorax complexes has been implicated in embryonic stem cell (ESC) self-renewal and differentiation. It has been shown recently that WRD5 and Dpy-30, specific components of the SET1/MLL protein complexes, play important roles during ESC self-renewal and differentiation of neural lineages. However, not much is known about how and where specific trithorax complexes are targeted to genes involved in self-renewal or lineage-specification. Here, we report that the recruitment of the hSET1A histone H3K4 methyltransferase (HMT) complex by transcription factor USF1 is required for mesoderm specification and lineage differentiation. In undifferentiated ESCs, USF1 maintains hematopoietic stem/progenitor cell (HS/PC) associated bivalent chromatin domains and differentiation potential. Furthermore, USF1 directed recruitment of the hSET1A complex to the HoxB4 promoter governs the transcriptional activation of HoxB4 gene and regulates the formation of early hematopoietic cell populations. Disruption of USF or hSET1A function by overexpression of a dominant-negative AUSF1 mutant or by RNA-interference-mediated knockdown, respectively, led to reduced expression of mesoderm markers and inhibition of lineage differentiation. We show that USF1 and hSET1A together regulate H3K4me3 modifications and transcription preinitiation complex assembly at the hematopoietic-associated HoxB4 gene during differentiation. Finally, ectopic expression of USF1 in ESCs promotes mesoderm differentiation and enforces the endothelial-to-hematopoietic transition by inducing hematopoietic-associated transcription factors, HoxB4 and TAL1. Taken together, our findings reveal that the guided-recruitment of the hSET1A histone methyltransferase complex and its H3K4 methyltransferase activity by transcription regulator USF1 safeguards hematopoietic transcription programs and enhances mesoderm/hematopoietic differentiation.http://europepmc.org/articles/PMC3675019?pdf=render
spellingShingle Changwang Deng
Ying Li
Shermi Liang
Kairong Cui
Tal Salz
Hui Yang
Zhanyun Tang
Patrick G Gallagher
Yi Qiu
Robert Roeder
Keji Zhao
Jörg Bungert
Suming Huang
USF1 and hSET1A mediated epigenetic modifications regulate lineage differentiation and HoxB4 transcription.
PLoS Genetics
title USF1 and hSET1A mediated epigenetic modifications regulate lineage differentiation and HoxB4 transcription.
title_full USF1 and hSET1A mediated epigenetic modifications regulate lineage differentiation and HoxB4 transcription.
title_fullStr USF1 and hSET1A mediated epigenetic modifications regulate lineage differentiation and HoxB4 transcription.
title_full_unstemmed USF1 and hSET1A mediated epigenetic modifications regulate lineage differentiation and HoxB4 transcription.
title_short USF1 and hSET1A mediated epigenetic modifications regulate lineage differentiation and HoxB4 transcription.
title_sort usf1 and hset1a mediated epigenetic modifications regulate lineage differentiation and hoxb4 transcription
url http://europepmc.org/articles/PMC3675019?pdf=render
work_keys_str_mv AT changwangdeng usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT yingli usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT shermiliang usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT kairongcui usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT talsalz usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT huiyang usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT zhanyuntang usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT patrickggallagher usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT yiqiu usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT robertroeder usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT kejizhao usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT jorgbungert usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription
AT suminghuang usf1andhset1amediatedepigeneticmodificationsregulatelineagedifferentiationandhoxb4transcription