Physiol. Genomics Ad Instruments
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Physiol. Genomics 7: 115-126, 2001. First published September 21, 2001; doi:10.1152/physiolgenomics.00013.2001
1094-8341/01 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
7/2/115    most recent
00013.2001v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Web of Science (2)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by NGIMBOUS, B. B.
Right arrow Articles by MOALIC, J.-M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by NGIMBOUS, B. B.
Right arrow Articles by MOALIC, J.-M.
Received 26 February 2001; accepted in final form 4 September 2001.
Physiological Genomics 7:115-126 (2001)
1094-8341/01 $5.00 © 2001 American Physiological Society

Heart transplantation changes the expression of distinct gene families

BEDEL BIYIHA NGIMBOUS 1, FRANCINE BOURGEOIS 2, CHRISTOPHE MAS 2, MICHEL SIMONNEAU 2 and JEAN-MARIE MOALIC 1

1 Unité 127, Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital Lariboisière, 75475 Paris Cedex
2 Neurogénétique/INSERM E9935, Hôpital Robert Debré, 75019 Paris, France

We took advantage of the combination of a rat heart transplantation model with a modified differential display RT-PCR method to identify transcriptome changes in the right atria from transplanted compared with native hearts. Based on sequence homology search, the 37 cDNAs differentially displayed both 2 and 7 days posttransplantation were categorized into 7 unknown transcripts, 16 expressed sequence tags (ESTs), and 14 partially or completely characterized genes. The last group cDNAs, validated by relative RT-PCR, belonged to diverse gene families involved in specific metabolisms, protein synthesis, cell signaling, and transcription. Furthermore, we identified differential transcripts corresponding to denervation and fetal gene reexpression. We found coordinate downregulation of genes involved in energy metabolism and protein synthesis regulation, similar to that reported for senescent skeletal muscle. From these transcriptome changes, we propose that heart transplants and senescent muscles share common molecular mechanisms.

heart transplantation; differential display; cardiac denervation; expression profile homologies







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online