Literature DB >> 20214951

Interaction of MTG family proteins with NEUROG2 and ASCL1 in the developing nervous system.

Joshua D Aaker1, Andrea L Patineau, Hyun-Jin Yang, David T Ewart, Yasushi Nakagawa, Steven C McLoon, Naoko Koyano-Nakagawa.   

Abstract

During neural development, members of MTG family of transcriptional repressors are induced by proneural basic helix-loop-helix (bHLH) transcription factors and in turn inhibit the activity of the bHLH proteins, forming a negative feedback loop that regulates the normal progression of neurogenesis. Three MTG genes, MTG8, MTG16 and MTGR1, are expressed in distinct patterns in the developing nervous system. Various bHLH proteins are also expressed in distinct patterns. We asked whether there is a functional relationship between specific MTG and bHLH proteins in developing chick spinal cord. First, we examined if each MTG gene is induced by specific bHLH proteins. Although expression of NEUROG2, ASCL1 and MTG genes overlapped, the boundaries of gene expression did not match. Ectopic expression analysis showed that MTGR1 and NEUROD4, which show similar expression patterns, are regulated differently by NEUROG2 and ASCL1. Thus, our results show that expression of MTG genes is not regulated by a single upstream bHLH protein, but represents an integration of the activity of multiple regulators. Next, we asked if each MTG protein inhibits specific bHLH proteins. Transcription assay showed that NEUROG2 and ASCL1 are inhibited by MTGR1 and MTG16, and less efficiently by MTG8. Deletion mapping of MTGR1 showed that MTGR1 binds NEUROG2 and ASCL1 using multiple interaction surfaces, and all conserved domains are required for its repressor activity. These results support the model that MTG proteins form a higher-order repressor complex and modulate transcriptional activity of bHLH proteins during neurogenesis. Copyright 2010 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20214951      PMCID: PMC2862279          DOI: 10.1016/j.neulet.2010.03.004

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  19 in total

Review 1.  ETO interacting proteins.

Authors:  Bruce A Hug; Mitchell A Lazar
Journal:  Oncogene       Date:  2004-05-24       Impact factor: 9.867

Review 2.  The MTG proteins: chromatin repression players with a passion for networking.

Authors:  Stefano Rossetti; André T Hoogeveen; Nicoletta Sacchi
Journal:  Genomics       Date:  2004-07       Impact factor: 5.736

3.  The expression and function of MTG/ETO family proteins during neurogenesis.

Authors:  Naoko Koyano-Nakagawa; Chris Kintner
Journal:  Dev Biol       Date:  2005-02-01       Impact factor: 3.582

4.  Gene expression of MASH-1, MATH-1, neuroD and NSCL-2, basic helix-loop-helix proteins, during neural differentiation in P19 embryonal carcinoma cells.

Authors:  F Itoh; T Nakane; S Chiba
Journal:  Tohoku J Exp Med       Date:  1997-08       Impact factor: 1.848

5.  Gene targeting reveals a crucial role for MTG8 in the gut.

Authors:  F Calabi; R Pannell; G Pavloska
Journal:  Mol Cell Biol       Date:  2001-08       Impact factor: 4.272

6.  XETOR regulates the size of the proneural domain during primary neurogenesis in Xenopus laevis.

Authors:  Ying Cao; Hui Zhao; Horst Grunz
Journal:  Mech Dev       Date:  2002-11       Impact factor: 1.882

7.  E protein silencing by the leukemogenic AML1-ETO fusion protein.

Authors:  Jinsong Zhang; Markus Kalkum; Soichiro Yamamura; Brian T Chait; Robert G Roeder
Journal:  Science       Date:  2004-08-27       Impact factor: 47.728

Review 8.  The ETO (MTG8) gene family.

Authors:  J Nathan Davis; Laura McGhee; Shari Meyers
Journal:  Gene       Date:  2003-01-16       Impact factor: 3.688

9.  Feedback regulation of NEUROG2 activity by MTGR1 is required for progression of neurogenesis.

Authors:  Joshua D Aaker; Andrea L Patineau; Hyun-Jin Yang; David T Ewart; Wuming Gong; Tongbin Li; Yasushi Nakagawa; Steven C McLoon; Naoko Koyano-Nakagawa
Journal:  Mol Cell Neurosci       Date:  2009-07-28       Impact factor: 4.314

10.  Induction and repression of mammalian achaete-scute homologue (MASH) gene expression during neuronal differentiation of P19 embryonal carcinoma cells.

Authors:  J E Johnson; K Zimmerman; T Saito; D J Anderson
Journal:  Development       Date:  1992-01       Impact factor: 6.868

View more
  6 in total

1.  Transient expression of Ngn3 in Xenopus endoderm promotes early and ectopic development of pancreatic beta and delta cells.

Authors:  Daniel Oropeza; Marko Horb
Journal:  Genesis       Date:  2012-01-30       Impact factor: 2.487

2.  Endothelial angiogenesis is directed by RUNX1T1-regulated VEGFA, BMP4 and TGF-β2 expression.

Authors:  Ko-Hsun Liao; Shing-Jyh Chang; Hsin-Chuan Chang; Chen-Li Chien; Tse-Shun Huang; Te-Chia Feng; Wen-Wei Lin; Chuan-Chi Shih; Muh-Hwa Yang; Shung-Haur Yang; Chi-Hung Lin; Wei-Lun Hwang; Oscar K Lee
Journal:  PLoS One       Date:  2017-06-22       Impact factor: 3.240

3.  Ascl1 Coordinately Regulates Gene Expression and the Chromatin Landscape during Neurogenesis.

Authors:  Alexandre A S F Raposo; Francisca F Vasconcelos; Daniela Drechsel; Corentine Marie; Caroline Johnston; Dirk Dolle; Angela Bithell; Sébastien Gillotin; Debbie L C van den Berg; Laurence Ettwiller; Paul Flicek; Gregory E Crawford; Carlos M Parras; Benedikt Berninger; Noel J Buckley; François Guillemot; Diogo S Castro
Journal:  Cell Rep       Date:  2015-03-05       Impact factor: 9.423

4.  Runx1t1 promotes the neuronal differentiation in rat hippocampus.

Authors:  Linqing Zou; Haoming Li; Xiao Han; Jianbing Qin; Guoqi Song
Journal:  Stem Cell Res Ther       Date:  2020-04-22       Impact factor: 6.832

5.  MTG8 interacts with LHX6 to specify cortical interneuron subtype identity.

Authors:  Zeinab Asgarian; Marcio Guiomar Oliveira; Agata Stryjewska; Ioannis Maragkos; Anna Noren Rubin; Lorenza Magno; Vassilis Pachnis; Mohammadmersad Ghorbani; Scott Wayne Hiebert; Myrto Denaxa; Nicoletta Kessaris
Journal:  Nat Commun       Date:  2022-09-05       Impact factor: 17.694

6.  Genome-wide association study identifies CBFA2T3 affecting the rate of CSF Aβ42 decline in non-demented elders.

Authors:  Kai-Xin Dou; Can Zhang; Chen-Chen Tan; Wei Xu; Jie-Qiong Li; Xi-Peng Cao; Lan Tan; Jin-Tai Yu
Journal:  Aging (Albany NY)       Date:  2019-08-01       Impact factor: 5.682

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.