Identification of genes expressed during myocardial development

Objective To identify genes expressed in the fetal heart that are potentially important for myocardial development and cardiomyocyte proliferation.Methods mRNAs from fetal (29 weeks ) and adult cardiomyocytes were use for suppression subtractive hybridization (SSH). Both forward (fetal as tester) an...

Full description

Saved in:
Bibliographic Details
Published inChinese medical journal Vol. 116; no. 9; pp. 1329 - 1332
Main Author 陈小圆 陈健宏 张丘琪 梁瑛 梁平
Format Journal Article
LanguageEnglish
Published China Department of Paediatrics and Adolescent Medicine, Laboratory Block, Faculty of Medicine Building, The University of Hong Kong, Hong Kong SAR, China 01.09.2003
Subjects
Online AccessGet full text
ISSN0366-6999
2542-5641

Cover

More Information
Summary:Objective To identify genes expressed in the fetal heart that are potentially important for myocardial development and cardiomyocyte proliferation.Methods mRNAs from fetal (29 weeks ) and adult cardiomyocytes were use for suppression subtractive hybridization (SSH). Both forward (fetal as tester) and reverse (adult as driver)subtractions were performed. Clones confirmed by dot-blot analysis to be differentially expressed were sequenced and analyzed.Results Differential expressions were detected for 39 out of 96 (41%) clones on forward subtraction and 24 out of 80 (30%) clones on reverse. For fetal dominating genes, 28 clones matched to 10known genes (COLIA2, COL3A1, endomucin, HBG1, HBG2, PCBP2, LOC51144, TGFBI, vinculin and PND), 9 clones to 5 cDNAs of unknown functions ( accession AK021715, AF085867, AB040948,AB051460 and AB051512 ) and 2 clones had homology to hEST sequences. For the reverse subtraction, all clones showed homology to mitochondrial transcripts.Conclusions We successfully applied SSH to detect those genes differentially expressed in fetal cardiac myocytes, some of which have not been shown relative to myocardial development.
Bibliography:11-2154/R
R331.31
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0366-6999
2542-5641