MOLECULAR-CLONING OF A PUTATIVE NOVEL HUMAN BZIP TRANSCRIPTION FACTOR ON CHROMOSOME 17Q22

被引:82
作者
LUNA, L
JOHNSEN, O
SKARTLIEN, AH
PEDEUTOUR, F
TURCCAREL, C
PRYDZ, H
KOLSTO, AB
机构
[1] UNIV OSLO,OSLO BIOTECHNOL CTR,N-0317 OSLO,NORWAY
[2] UNIV NICE,CNRS,CANC CYTOGENET LAB,URA 1462,F-06107 NICE,FRANCE
关键词
D O I
10.1006/geno.1994.1428
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have cloned and characterized cDNA clones representing several mRNA isoforms generated by alternative splicing of a single gene localized to chromosome 17q22. Sequence analysis showed that the predicted translational product of the longest open reading frame (2316 nucleotides, 772 amino acids) is related to transcription factors of the basic leucine zipper (bZIP) class. The sequence contained several regions characteristic of transcriptional regulatory domains. A cluster of amino acids flanking the bZIP region on both sides was highly conserved between TCF11 and p45 NF-E2, a subunit of the human globin locus control region-binding protein, NF-E2. These same regions showed remarkable homology to two invertebrate proteins, CNC and skn-1, postulated to regulate embryonic development in Drosophila melanogaster and Caenorhabditis elegans, respectively. (C) 1994 Academic Press, Inc.
引用
收藏
页码:553 / 562
页数:10
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