CDNA CLONING AND GENOMIC ORGANIZATION OF ENHANCER OF SPLIT GROUCHO GENE FROM NEMATODE CAENORHABDITIS-ELEGANS

Citation
Fs. Sharief et al., CDNA CLONING AND GENOMIC ORGANIZATION OF ENHANCER OF SPLIT GROUCHO GENE FROM NEMATODE CAENORHABDITIS-ELEGANS, Biochemistry and molecular biology international, 43(2), 1997, pp. 327-337
Citations number
22
ISSN journal
10399712
Volume
43
Issue
2
Year of publication
1997
Pages
327 - 337
Database
ISI
SICI code
1039-9712(1997)43:2<327:CCAGOO>2.0.ZU;2-Z
Abstract
This first genomic Enhancer of split groucho (ESG) gene and its full l ength complementary DNA (cDNA) from nematode C. elegans were cloned an d sequenced via homology with the corresponding Drosophila groucho cDN A. The cDNA of 2.1-Kb encodes a protein of 612 amino acids, and the ne matode ESG protein is the smallest and most different in structure com pared to all ESG related proteins. The gene isolated is 4,246-bp in si ze, including 1,219-bp promoter region. A putative TATA-box at positio n -1166, two consensus sequence of ACTGG, characteristic of leader bin ding protein-1 (LBP-1) binding motifs at position -563 and -211 and ni ne CAAT boxes were found in the promoter region of ESG gene. The prote in-coding sequence is interrupted by five introns. The length of intro ns 1 to 5 is 52, 252, 87, 53 and 518 bp, respectively. The overall str uctural relationships of the ESG-related proteins among human, mouse, rat, Xenopus, Drosophila and nematode were also analyzed.