Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters











Database
Language
Publication year range
1.
Mech Dev ; 103(1-2): 79-91, 2001 May.
Article in English | MEDLINE | ID: mdl-11335114

ABSTRACT

Chicken embryonic stem (CES) cells are pluripotent cells derived from chicken early blastoderm. In order to identify new genes specifically expressed in these pluripotent cells, we have used a gene trap strategy and cloned a novel gene family called cENS for chicken Embryonic Normal Stem cell gene. The cENS genes expression decreases after induction of CES cells differentiation in culture and is restricted in vivo to the very early embryo. We have characterized three different cENS genes. One, cENS-1, is composed of an open reading frame inserted between two terminal direct repeats which are the common point of the cENS genes. cENS-1 encodes a protein identical to cERNI, a recently described protein. cENS-2 is a truncated form of cENS-1. cENS-3 presents two adjacent open reading frames coding respectively for env and pol related proteins. The presence of conserved direct repeats, of retrovirus related genes and the absence of introns argue in favor of a retroviral origin of the cENS genes. In the cENS we identified a promoter region whose activity is strong in CES cells and decreases after induced differentiation showing a highly specific transcriptional activity specific of undifferentiated chicken embryonic stem cells.


Subject(s)
Avian Proteins , Embryo, Nonmammalian/metabolism , Fetal Proteins/genetics , Multigene Family , Alleles , Amino Acid Sequence , Animals , Base Sequence , Cell Differentiation , Cell Lineage , Cells, Cultured , Chick Embryo , DNA/metabolism , DNA, Complementary/metabolism , Fetal Proteins/biosynthesis , Genes, Reporter , In Situ Hybridization , Introns , Luciferases/metabolism , Models, Genetic , Molecular Sequence Data , Open Reading Frames , Promoter Regions, Genetic , RNA/metabolism , RNA, Messenger/metabolism , Retroviridae/genetics , Reverse Transcriptase Polymerase Chain Reaction , Sequence Homology, Amino Acid , Time Factors , Tissue Distribution , Transcription, Genetic , Transfection , beta-Galactosidase/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL