Home LiteratureArticle Details
PMID: 11395543 Published · epublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Divergent transcriptional responses to independent genetic causes of cardiac hypertrophy.

Physiological genomics ·Vol. 6 ·No. 1 ·2001-06-06 ·Pages 19-28

Aronow BJ, Toyokawa T, Canning A, Haghighi K, Delling U, Kranias E, Molkentin JD, Dorn GW

Abstract

To define molecular mechanisms of cardiac hypertrophy, genes whose expression was perturbed by any of four different transgenic mouse hypertrophy models [protein kinase C-epsilon activation peptide (PsiepsilonRACK), calsequestrin (CSQ), calcineurin (CN), and Galpha(q)] were compared by DNA microarray analyses using the approximately 8,800 genes present on the Incyte mouse GEM1. The total numbers of regulated genes (tens to hundreds) correlated with phenotypic severity of the model (Galpha(q) > CN > CSQ > PsiepsilonRACK), but demonstrated that no single gene was consistently upregulated. Of the three models exhibiting pathological hypertrophy, only atrial natriuretic peptide was consistently upregulated, suggesting that transcriptional alterations are highly specific to individual genetic causes of hypertrophy. However, hierarchical-tree and K-means clustering analyses revealed that subsets of the upregulated genes did exhibit coordinate regulatory patterns that were unique or overlapping across the different hypertrophy models. One striking set consisted of apoptotic genes uniquely regulated in the apoptosis-prone Galpha(q) model. Thus, rather than identifying a single common hypertrophic cardiomyopathy gene program, these data suggest that extensive groups of genes may be useful for the prediction of specific underlying genetic determinants and condition-specific therapeutic approaches.

MeSH Terms
Animals Apoptosis/genetics Calcineurin/genetics Calsequestrin/genetics Cardiomegaly/genetics,metabolism GTP-Binding Protein alpha Subunits, Gq-G11 Gene Expression Profiling Heterotrimeric GTP-Binding Proteins/genetics Isoenzymes/metabolism Mice Mice, Transgenic Oligonucleotide Array Sequence Analysis Protein Kinase C/metabolism Protein Kinase C-epsilon RNA, Messenger/biosynthesis Transcription, Genetic Up-Regulation
Chemicals
Calsequestrin Isoenzymes RNA, Messenger Prkce protein, mouse Protein Kinase C Protein Kinase C-epsilon Calcineurin GTP-Binding Protein alpha Subunits, Gq-G11 Heterotrimeric GTP-Binding Proteins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Aronow B J
Department of Developmental Biology, Children's Hospital Research Center, Cincinnati, OH 45229, USA.
Toyokawa T
Canning A
Haghighi K
Delling U
Kranias E
Molkentin J D
Dorn G W
Article Info
Journal
Physiological genomics
Abbr.
Physiol Genomics
ISSN
1531-2267
Published
2001-06-06
Epub
2001-00-06
Pages
19-28
Language
English
Region
United States
NLM ID
9815683
Subset
IM
Grants
NIEHS NIH HHS · ES-08822 · United States
NHLBI NIH HHS · HL-26057 · United States
NHLBI NIH HHS · HL-52318 · United States
NHLBI NIH HHS · HL-58010 · United States
NHLBI NIH HHS · HL-64018 · United States
NHLBI NIH HHS · HL/HD-59888 · United States
OCPHP CDC HHS · P40-PR-13358 · United States
Corrections
CommentIn
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com