Literature DB >> 22449848

MicroRNAs in heart development.

Ramón A Espinoza-Lewis1, Da-Zhi Wang.   

Abstract

MicroRNAs (miRNAs) are a class of small noncoding RNAs of ~22nt in length which are involved in the regulation of gene expression at the posttranscriptional level by degrading their target mRNAs and/or inhibiting their translation. Expressed ubiquitously or in a tissue-specific manner, miRNAs are involved in the regulation of many biological processes such as cell proliferation, differentiation, apoptosis, and the maintenance of normal cellular physiology. Many miRNAs are expressed in embryonic, postnatal, and adult hearts. Aberrant expression or genetic deletion of miRNAs is associated with abnormal cardiac cell differentiation, disruption of heart development, and cardiac dysfunction. This chapter will summarize the history, biogenesis, and processing of miRNAs as well as their function in heart development, remodeling, and disease.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22449848      PMCID: PMC4888772          DOI: 10.1016/B978-0-12-387786-4.00009-9

Source DB:  PubMed          Journal:  Curr Top Dev Biol        ISSN: 0070-2153            Impact factor:   4.897


  172 in total

1.  Activation of cardiac gene expression by myocardin, a transcriptional cofactor for serum response factor.

Authors:  D Wang; P S Chang; Z Wang; L Sutherland; J A Richardson; E Small; P A Krieg; E N Olson
Journal:  Cell       Date:  2001-06-29       Impact factor: 41.582

2.  An intragenic MEF2-dependent enhancer directs muscle-specific expression of microRNAs 1 and 133.

Authors:  Ning Liu; Andrew H Williams; Yuri Kim; John McAnally; Svetlana Bezprozvannaya; Lillian B Sutherland; James A Richardson; Rhonda Bassel-Duby; Eric N Olson
Journal:  Proc Natl Acad Sci U S A       Date:  2007-12-19       Impact factor: 11.205

Review 3.  Selective nuclear export mechanism of small RNAs.

Authors:  Soo Jae Lee; Chimari Jiko; Eiki Yamashita; Tomitake Tsukihara
Journal:  Curr Opin Struct Biol       Date:  2010-12-07       Impact factor: 6.809

4.  MicroRNA-1 regulates smooth muscle cell differentiation by repressing Kruppel-like factor 4.

Authors:  Changqing Xie; Huarong Huang; Xuan Sun; Yanhong Guo; Milton Hamblin; Raquel P Ritchie; Minerva T Garcia-Barrio; Jifeng Zhang; Y Eugene Chen
Journal:  Stem Cells Dev       Date:  2010-10-18       Impact factor: 3.272

5.  tinman-related genes expressed during heart development in Xenopus.

Authors:  C S Newman; P A Krieg
Journal:  Dev Genet       Date:  1998

6.  Expression of microRNAs is dynamically regulated during cardiomyocyte hypertrophy.

Authors:  Mariko Tatsuguchi; Hee Young Seok; Thomas E Callis; J Michael Thomson; Jian-Fu Chen; Martin Newman; Mauricio Rojas; Scott M Hammond; Da-Zhi Wang
Journal:  J Mol Cell Cardiol       Date:  2007-04-14       Impact factor: 5.000

7.  An endogenous small interfering RNA pathway in Drosophila.

Authors:  Benjamin Czech; Colin D Malone; Rui Zhou; Alexander Stark; Catherine Schlingeheyde; Monica Dus; Norbert Perrimon; Manolis Kellis; James A Wohlschlegel; Ravi Sachidanandam; Gregory J Hannon; Julius Brennecke
Journal:  Nature       Date:  2008-05-07       Impact factor: 49.962

8.  The transcriptional repressor Tbx3 delineates the developing central conduction system of the heart.

Authors:  Willem M H Hoogaars; Alessandra Tessari; Antoon F M Moorman; Piet A J de Boer; Jaco Hagoort; Alexandre T Soufan; Marina Campione; Vincent M Christoffels
Journal:  Cardiovasc Res       Date:  2004-06-01       Impact factor: 10.787

9.  Dicer is essential for mouse development.

Authors:  Emily Bernstein; Sang Yong Kim; Michelle A Carmell; Elizabeth P Murchison; Heather Alcorn; Mamie Z Li; Alea A Mills; Stephen J Elledge; Kathryn V Anderson; Gregory J Hannon
Journal:  Nat Genet       Date:  2003-10-05       Impact factor: 38.330

10.  Genome-wide identification, organization and phylogenetic analysis of Dicer-like, Argonaute and RNA-dependent RNA Polymerase gene families and their expression analysis during reproductive development and stress in rice.

Authors:  Meenu Kapoor; Rita Arora; Tenisha Lama; Aashima Nijhawan; Jitendra P Khurana; Akhilesh K Tyagi; Sanjay Kapoor
Journal:  BMC Genomics       Date:  2008-10-01       Impact factor: 3.969

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  33 in total

1.  LincRNA-p21 regulates neointima formation, vascular smooth muscle cell proliferation, apoptosis, and atherosclerosis by enhancing p53 activity.

Authors:  Gengze Wu; Jin Cai; Yu Han; Jinghai Chen; Zhan-Peng Huang; Caiyu Chen; Yue Cai; Hefei Huang; Yujia Yang; Yukai Liu; Zaicheng Xu; Duofen He; Xiaoqun Zhang; Xiaoyun Hu; Luca Pinello; Dan Zhong; Fengtian He; Guo-Cheng Yuan; Da-Zhi Wang; Chunyu Zeng
Journal:  Circulation       Date:  2014-08-25       Impact factor: 29.690

2.  Loss of MicroRNA-155 protects the heart from pathological cardiac hypertrophy.

Authors:  Hee Young Seok; Jinghai Chen; Masaharu Kataoka; Zhan-Peng Huang; Jian Ding; Jinglu Yan; Xiaoyun Hu; Da-Zhi Wang
Journal:  Circ Res       Date:  2014-03-21       Impact factor: 17.367

3.  Let-7 family of microRNA is required for maturation and adult-like metabolism in stem cell-derived cardiomyocytes.

Authors:  Kavitha T Kuppusamy; Daniel C Jones; Henrik Sperber; Anup Madan; Karin A Fischer; Marita L Rodriguez; Lil Pabon; Wei-Zhong Zhu; Nathaniel L Tulloch; Xiulan Yang; Nathan J Sniadecki; Michael A Laflamme; Walter L Ruzzo; Charles E Murry; Hannele Ruohola-Baker
Journal:  Proc Natl Acad Sci U S A       Date:  2015-05-11       Impact factor: 11.205

4.  Functional annotation of differentially expressed fetal cardiac microRNA targets: implication for microRNA-based cardiovascular therapeutics.

Authors:  Sharad Saxena; Anubhuti Gupta; Vaibhav Shukla; Vibha Rani
Journal:  3 Biotech       Date:  2018-11-21       Impact factor: 2.406

5.  Multifaceted roles of miR-1s in repressing the fetal gene program in the heart.

Authors:  Yusheng Wei; Siwu Peng; Meng Wu; Ravi Sachidanandam; Zhidong Tu; Shihong Zhang; Christine Falce; Eric A Sobie; Djamel Lebeche; Yong Zhao
Journal:  Cell Res       Date:  2014-01-31       Impact factor: 25.617

Review 6.  Long-term consequences of disrupting adenosine signaling during embryonic development.

Authors:  Scott A Rivkees; Christopher C Wendler
Journal:  Mol Aspects Med       Date:  2017-02-13

7.  MiR-135b is a direct PAX6 target and specifies human neuroectoderm by inhibiting TGF-β/BMP signaling.

Authors:  Akshay Bhinge; Jeremie Poschmann; Seema C Namboori; Xianfeng Tian; Sharon Jia Hui Loh; Anna Traczyk; Shyam Prabhakar; Lawrence W Stanton
Journal:  EMBO J       Date:  2014-05-06       Impact factor: 11.598

8.  MicroRNA-22 regulates cardiac hypertrophy and remodeling in response to stress.

Authors:  Zhan-Peng Huang; Jinghai Chen; Hee Young Seok; Zheng Zhang; Masaharu Kataoka; Xiaoyun Hu; Da-Zhi Wang
Journal:  Circ Res       Date:  2013-03-22       Impact factor: 17.367

Review 9.  miR-22 in cardiac remodeling and disease.

Authors:  Zhan-Peng Huang; Da-Zhi Wang
Journal:  Trends Cardiovasc Med       Date:  2014-08-02       Impact factor: 6.677

10.  Loss of microRNA-22 prevents high-fat diet induced dyslipidemia and increases energy expenditure without affecting cardiac hypertrophy.

Authors:  Gabriela Placoná Diniz; Zhan-Peng Huang; Jianming Liu; Jinghai Chen; Jian Ding; Renata Inzinna Fonseca; Maria Luiza Barreto-Chaves; Jose Donato; Xiaoyun Hu; Da-Zhi Wang
Journal:  Clin Sci (Lond)       Date:  2017-12-04       Impact factor: 6.124

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