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Smyd1 is essential for myosin expression and sarcomere organization in craniofacial, extraocular, and cardiac muscles
Jiao, Shuang1,2,3; Xu, Rui1; Du, Shaojun1
2021-03-20
发表期刊JOURNAL OF GENETICS AND GENOMICS
ISSN1673-8527
卷号48期号:3页码:208-218
通讯作者Du, Shaojun([email protected])
摘要Skeletal and cardiac muscles are striated myofibers that contain highly organized sarcomeres for muscle contraction. Recent studies revealed that Smyd1, a lysine methyltransferase, plays a key role in sarcomere assembly in heart and trunk skeletal muscles. However, Smyd1 expression and function in craniofacial muscles are not known. Here, we analyze the developmental expression and function of two smyd1 paralogous genes, smyd1a and smyd1b, in craniofacial and cardiac muscles of zebrafish embryos. Our data show that loss of smyd1a (smyd1a(mb5)) or smyd1b (smyd1b(sa15678)) has no visible effects on myogenic commitment and expression of myod and myosin heavy-chain mRNA transcripts in craniofacial muscles. However, myosin heavy-chain protein accumulation and sarcomere organization are dramatically reduced in smyd1b(sa15678) single mutant, and almost completely diminish in smyd1a(mb5); smyd1b(sa15678) double mutant, but not in smyd1a(mb5) mutant. Similar defects are also observed in cardiac muscles of smyd1b(sa15678) mutant. Defective craniofacial and cardiac muscle formation is associated with an upregulation of hsp90 alpha 1 and unc45b mRNA expression in smyd1b(sa15678) and smyd1a(mb5); smyd1b(sa15678) mutants. Together, our studies indicate that Smyd1b, but not Smyd1a, plays a key role in myosin heavy-chain protein expression and sarcomere organization in craniofacial and cardiac muscles. Loss of smyd1b results in muscle-specific stress response. Copyright (C) 2021, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, and Genetics Society of China. Published by Elsevier Limited and Science Press. All rights reserved.
关键词Smyd1 Myosin Sarcomere Craniofacial muscle Cardiac muscle
DOI10.1016/j.jgg.2021.03.004
收录类别SCI
语种英语
资助项目U.S. National Institute of Health (NIH) National Institute of Arthritis and Musculoskeletal and Skin Diseases[R01AR072703]; China Scholarship Council
WOS研究方向Biochemistry & Molecular Biology ; Genetics & Heredity
WOS类目Biochemistry & Molecular Biology ; Genetics & Heredity
WOS记录号WOS:000681047800004
出版者SCIENCE PRESS
引用统计
被引频次:9[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/175990
专题实验海洋生物学重点实验室
通讯作者Du, Shaojun
作者单位1.Univ Maryland, Inst Marine & Environm Technol, Sch Med, Dept Biochem & Mol Biol, Baltimore, MD 21202 USA
2.Chinese Acad Sci, Ctr Ocean Megasci, Inst Oceanol, Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
3.Shandong Univ Technol, Sch Life Sci, Zibo 255049, Peoples R China
第一作者单位中国科学院海洋大科学研究中心
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GB/T 7714
Jiao, Shuang,Xu, Rui,Du, Shaojun. Smyd1 is essential for myosin expression and sarcomere organization in craniofacial, extraocular, and cardiac muscles[J]. JOURNAL OF GENETICS AND GENOMICS,2021,48(3):208-218.
APA Jiao, Shuang,Xu, Rui,&Du, Shaojun.(2021).Smyd1 is essential for myosin expression and sarcomere organization in craniofacial, extraocular, and cardiac muscles.JOURNAL OF GENETICS AND GENOMICS,48(3),208-218.
MLA Jiao, Shuang,et al."Smyd1 is essential for myosin expression and sarcomere organization in craniofacial, extraocular, and cardiac muscles".JOURNAL OF GENETICS AND GENOMICS 48.3(2021):208-218.
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