Physiol. Genomics Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Physiol. Genomics 16: 268-274, 2004; doi:10.1152/physiolgenomics.00167.2003
1094-8341/04 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
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 ISI 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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wesolowski, S. R.
Right arrow Articles by Ernst, C. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wesolowski, S. R.
Right arrow Articles by Ernst, C. W.
Received 30 September 2003; accepted in final form 13 November 2003.
Physiological Genomics 16:268-274 (2004)
1094-8341/04 $5.00 © 2004 American Physiological Society

Developmental changes in the fetal pig transcriptome

Stephanie R. Wesolowski, Nancy E. Raney and Catherine W. Ernst

Department of Animal Science, Michigan State University, East Lansing, Michigan 48824

Growth and development of pig fetuses is dependent on the coordinated expression of multiple genes. Between 21 and 45 days of gestation, fetuses experience increasing growth rates that can result in uterine crowding and increased mortality. We used differential display reverse transcription-PCR (DDRT-PCR) to identify differentially expressed genes in pig fetuses at 21, 35, and 45 days of gestation. Pig cDNAs were identified with homologies to CD3 {gamma}-subunit, collagen type XIV {alpha}1, complement component C6, craniofacial developmental protein 1, crystallin-{gamma}E, DNA binding protein B, {epsilon}-globin, formin binding protein 2, ribosomal protein L23, small acidic protein, secreted frizzled related protein 2, titin, vitamin D binding protein, and two hypothetical protein products. Two novel expressed sequence tags (ESTs) were also identified. Expression patterns were confirmed for eight genes, and spatiotemporal expression of three genes was evaluated. We identified novel transcriptome changes in fetal pigs during a period of rapid growth. These changes involved genes with a spectrum of proposed functions, including musculoskeletal growth, immune system function, and cellular regulation. This information can ultimately be used to enhance production efficiency through improved pig growth and survival.

differential display; Northern hybridization; spatial expression; fetal development




This article has been cited by other articles:


Home page
Physiol. GenomicsHome page
S. Ponsuksili, E. Murani, C. Walz, M. Schwerin, and K. Wimmers
Pre- and postnatal hepatic gene expression profiles of two pig breeds differing in body composition: insight into pathways of metabolic regulation
Physiol Genomics, May 11, 2007; 29(3): 267 - 279.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2004 by the American Physiological Society.