Literature DB >> 9007248

Mutations affecting the formation and function of the cardiovascular system in the zebrafish embryo.

D Y Stainier1, B Fouquet, J N Chen, K S Warren, B M Weinstein, S E Meiler, M A Mohideen, S C Neuhauss, L Solnica-Krezel, A F Schier, F Zwartkruis, D L Stemple, J Malicki, W Driever, M C Fishman.   

Abstract

As part of a large-scale mutagenesis screen of the zebrafish genome, we have identified 58 mutations that affect the formation and function of the cardiovascular system. The cardiovascular system is particularly amenable for screening in the transparent zebrafish embryo because the heart and blood vessels are prominent and their function easily examined. We have classified the mutations affecting the heart into those that affect primarily either morphogenesis or function. Nine mutations clearly disrupt the formation of the heart. cloche deletes the endocardium. In cloche mutants, the myocardial layer forms in the absence of the endocardium but is dysmorphic and exhibits a weak contractility. Two loci, miles apart and bonnie and clyde, play a critical role in the fusion of the bilateral tubular primordia. Three mutations lead to an abnormally large heart and one to the formation of a diminutive, dysmorphic heart. We have found no mutation that deletes the myocardial cells altogether, but one, pandora, appears to eliminate the ventricle selectively. Seven mutations interfere with vascular integrity, as indicated by hemorrhage at particular sites. In terms of cardiac function, one large group exhibits a weak beat. In this group, five loci affect both chambers and seven a specific chamber (the atrium or ventricle). For example, the weak atrium mutation exhibits an atrium that becomes silent but has a normally beating ventricle. Seven mutations affect the rhythm of the heart causing, for example, a slow rate, a fibrillating pattern or an apparent block to conduction. In several other mutants, regurgitation of blood flow from ventricle to atrium is the most prominent abnormality, due either to the absence of valves or to poor coordination between the chambers with regard to the timing of contraction. The mutations identified in this screen point to discrete and critical steps in the formation and function of the heart and vasculature.

Entities:  

Mesh:

Year:  1996        PMID: 9007248     DOI: 10.1242/dev.123.1.285

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  174 in total

Review 1.  Zebrafish genetics: the enigma of arrival.

Authors:  M C Fishman
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-14       Impact factor: 11.205

2.  The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development.

Authors:  F A Pereira; Y Qiu; G Zhou; M J Tsai; S Y Tsai
Journal:  Genes Dev       Date:  1999-04-15       Impact factor: 11.361

3.  Small molecule developmental screens reveal the logic and timing of vertebrate development.

Authors:  R T Peterson; B A Link; J E Dowling; S L Schreiber
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-21       Impact factor: 11.205

Review 4.  The molecular basis of cardiac arrhythmias.

Authors:  Kalyanam Shivkumar; Narayana S Murali; Subramaniam C Krishnan
Journal:  J Nucl Cardiol       Date:  2002 Mar-Apr       Impact factor: 5.952

5.  Ccm1 regulates microvascular morphogenesis during angiogenesis.

Authors:  Huiling Liu; Daniele Rigamonti; Ahmed Badr; Jun Zhang
Journal:  J Vasc Res       Date:  2010-10-07       Impact factor: 1.934

6.  Distinct troponin C isoform requirements in cardiac and skeletal muscle.

Authors:  Vanessa M Sogah; Fabrizio C Serluca; Mark C Fishman; Deborah L Yelon; Calum A Macrae; John D Mably
Journal:  Dev Dyn       Date:  2010-11       Impact factor: 3.780

7.  Sensitivity to dioxin decreases as zebrafish mature.

Authors:  Kevin A Lanham; Richard E Peterson; Warren Heideman
Journal:  Toxicol Sci       Date:  2012-03-08       Impact factor: 4.849

8.  Production of maternal-zygotic mutant zebrafish by germ-line replacement.

Authors:  Brian Ciruna; Gilbert Weidinger; Holger Knaut; Bernard Thisse; Christine Thisse; Erez Raz; Alexander F Schier
Journal:  Proc Natl Acad Sci U S A       Date:  2002-10-23       Impact factor: 11.205

9.  A betaPix Pak2a signaling pathway regulates cerebral vascular stability in zebrafish.

Authors:  Jing Liu; Sherri D Fraser; Patrick W Faloon; Evvi Lynn Rollins; Johannes Vom Berg; Olivera Starovic-Subota; Angie L Laliberte; Jau-Nian Chen; Fabrizio C Serluca; Sarah J Childs
Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-15       Impact factor: 11.205

10.  pak2a mutations cause cerebral hemorrhage in redhead zebrafish.

Authors:  David A Buchner; Fengyun Su; Jennifer S Yamaoka; Makoto Kamei; Jordan A Shavit; Linda K Barthel; Beth McGee; Julio D Amigo; Seongcheol Kim; Andrew W Hanosh; Pudur Jagadeeswaran; Daniel Goldman; Nathan D Lawson; Pamela A Raymond; Brant M Weinstein; David Ginsburg; Susan E Lyons
Journal:  Proc Natl Acad Sci U S A       Date:  2007-08-22       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.