Molecular Cloning of a Putative Novel Human bZIP Transcription Factor on Chromosome 17q22

We have cloned and characterized cDNA clones representing several mRNA isoforms generated by alternative splicing of a single gene localized to chromosome some 17q22. Sequence analysis showed that the predicted translational product of the longest open reading frame (2316 nucleotides, 772 amino acid...

Full description

Saved in:
Bibliographic Details
Published inGenomics (San Diego, Calif.) Vol. 22; no. 3; pp. 553 - 562
Main Authors Luna, Luisa, Johnsen, Øyvind, Skartlien, Anne Helen, Pedeutour, Florence, Turc-Carel, Claude, Prydz, Hans, Kolstø, Anne-brit
Format Journal Article
LanguageEnglish
Published San Diego, CA Elsevier Inc 01.08.1994
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:We have cloned and characterized cDNA clones representing several mRNA isoforms generated by alternative splicing of a single gene localized to chromosome some 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.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0888-7543
1089-8646
DOI:10.1006/geno.1994.1428