Literature DB >> 25274780

Zebrafish cul4a, but not cul4b, modulates cardiac and forelimb development by upregulating tbx5a expression.

Xiaohan Zhao1, Baichun Jiang1, Huili Hu1, Fei Mao1, Jun Mi1, Zhaohui Li1, Qiji Liu1, Changshun Shao2, Yaoqin Gong2.   

Abstract

CUL4A and CUL4B are closely related cullin family members and can each assemble a Cullin-RING E3 ligase complex (CRL) and participate in a variety of biological processes. While the CRLs formed by the two cullin members may have common targets, the two appeared to have very different consequences when mutated or disrupted in mammals. We here investigated the roles of cul4a and cul4b during zebrafish embryogenesis by using the morpholino knockdown approach. We found that cul4a is essential for cardiac development as well as for pectoral fin development. Whereas cul4a morphants appeared to be unperturbed in chamber specification, they failed to undergo heart looping. The failures in heart looping and pectoral fin formation in cul4a morphants were accompanied by greatly reduced proliferation of cardiac cells and pectoral fin-forming cells. We demonstrated that tbx5a, a transcription factor essential for heart and limb development, is transcriptionally upregulated by cul4a and mediates the function of cul4a in cardiac and pectoral fin development. In contrast to the critical importance of cul4a, cul4b appeared to be dispensable for zebrafish development and was incapable of compensating for the loss of cul4a. This work provides the first demonstration of an essential role of cul4a, but not cul4b, in cardiac development and in the regulation of tbx5a in zebrafish. These findings justify exploring the functional role of CUL4A in human cardiac development.
© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

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Year:  2014        PMID: 25274780     DOI: 10.1093/hmg/ddu503

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  7 in total

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2.  p63 is a cereblon substrate involved in thalidomide teratogenicity.

Authors:  Tomoko Asatsuma-Okumura; Hideki Ando; Marco De Simone; Junichi Yamamoto; Tomomi Sato; Nobuyuki Shimizu; Kazuhide Asakawa; Yuki Yamaguchi; Takumi Ito; Luisa Guerrini; Hiroshi Handa
Journal:  Nat Chem Biol       Date:  2019-10-07       Impact factor: 15.040

Review 3.  Thalidomide-induced teratogenesis: history and mechanisms.

Authors:  Neil Vargesson
Journal:  Birth Defects Res C Embryo Today       Date:  2015-06-04

4.  Cul4a as a New Interaction Protein of PARP1 Inhibits Oxidative Stress-Induced H9c2 Cell Apoptosis.

Authors:  Ning Ye; Naijin Zhang; Ying Zhang; Hao Qian; Boquan Wu; Yingxian Sun
Journal:  Oxid Med Cell Longev       Date:  2019-04-17       Impact factor: 6.543

5.  Cul4a promotes zebrafish primitive erythropoiesis via upregulating scl and gata1 expression.

Authors:  Fan Yang; Huili Hu; Yuanyuan Liu; Ming Shao; Changshun Shao; Yaoqin Gong
Journal:  Cell Death Dis       Date:  2019-05-17       Impact factor: 8.469

6.  Loss of DDB1 Leads to Transcriptional p53 Pathway Activation in Proliferating Cells, Cell Cycle Deregulation, and Apoptosis in Zebrafish Embryos.

Authors:  Zhilian Hu; Jochen Holzschuh; Wolfgang Driever
Journal:  PLoS One       Date:  2015-07-30       Impact factor: 3.240

7.  CUL5 is required for thalidomide-dependent inhibition of cellular proliferation.

Authors:  Bryan Kunkler; Daniel Salamango; Zachary J DeBruine; Caitlin Ploch; Shirley Dean; David Grossens; Michael P Hledin; Gabriel A Marquez; Julie Madden; Abigayle Schnell; Michael Short; Maria A Burnatowska-Hledin
Journal:  PLoS One       Date:  2018-05-10       Impact factor: 3.240

  7 in total

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