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Gene Expression Profile Created for Mouse Stem Cells and Developing Embryo

Authors :
Alexei A. Sharov
Kazuhiro Aiba
Yulan Piao
Dan L. Longo
Janet Kelso
Yuxia Wang
Akihiro Umezawa
Michele D'Urso
Mark G. Carter
Patrick R. Martin
Hidenori Akutsu
Emily Klotz
Richard J. Hodes
Janet Rossant
Jonathan R. Keller
Yong Qian
Angelo L. Vescovi
Ramaiah Nagaraja
Lioudmila V. Sharova
Dawood B. Dudekula
Anna Curci
Wendy L. Kimber
Carole A. Stagg
Winston Hide
Tilo Kunath
Dennis D. Taub
Tetsuya S. Tanaka
Saied A. Jaradat
David Schlessinger
Kenneth R. Boheler
Vincent VanBuren
Brigid L.M. Hogan
Garnett Kelsoe
Serafino Pantano
Geppino Falco
Toshio Hamatani
Ryo Matoba
Toshiyuki Yoshikawa
Uwem C. Bassey
Minoru S.H. Ko
Source :
PLoS Biology, ResearcherID, PLoS Biology, Vol 1, Iss 3, p E74 (2003)
Publication Year :
2003
Publisher :
Public Library of Science (PLoS), 2003.

Abstract

Understanding and harnessing cellular potency are fundamental in biology and are also critical to the future therapeutic use of stem cells. Transcriptome analysis of these pluripotent cells is a first step towards such goals. Starting with sources that include oocytes, blastocysts, and embryonic and adult stem cells, we obtained 249,200 high-quality EST sequences and clustered them with public sequences to produce an index of approximately 30,000 total mouse genes that includes 977 previously unidentified genes. Analysis of gene expression levels by EST frequency identifies genes that characterize preimplantation embryos, embryonic stem cells, and adult stem cells, thus providing potential markers as well as clues to the functional features of these cells. Principal component analysis identified a set of 88 genes whose average expression levels decrease from oocytes to blastocysts, stem cells, postimplantation embryos, and finally to newborn tissues. This can be a first step towards a possible definition of a molecular scale of cellular potency. The sequences and cDNA clones recovered in this work provide a comprehensive resource for genes functioning in early mouse embryos and stem cells. The nonrestricted community access to the resource can accelerate a wide range of research, particularly in reproductive and regenerative medicine.<br />250,000 EST sequences from oocytes, blastocysts, and embryonic and adult stem cells contribute to the annotation of the mouse genome and suggest genes that contribute to the unique features of these developmental stages and cell types

Details

ISSN :
15457885 and 15449173
Volume :
1
Database :
OpenAIRE
Journal :
PLoS Biology
Accession number :
edsair.doi.dedup.....0ec6109970bca65456ab22f41eec09b1
Full Text :
https://doi.org/10.1371/journal.pbio.0000074