elt-2, a Second GATA Factor from the Nematode Caenorhabditis elegans(*)

  1. Mark G. Hawkins and
  2. James D. McGhee(§)
  1. From the (1)Department of Medical Biochemistry, University of Calgary, Calgary, Alberta, Canada T2N 4N1
  1. § To whom correspondence should be addressed:
    Dept. of Medical Biochemistry, University of Calgary, Health Sciences Centre, Rm. 2265, 3330 Hospital Drive N.W., Calgary, Alberta, Canada T2N 4N1.
    Tel.: 403-220-4476; Fax: 403-270-0737.

Abstract

We have previously shown that a tandem pair of (A/T)GATA(A/G) sequences in the promoter region of the Caenorhabditis elegans gut esterase gene (ges-1) controls the tissue specificity of ges-1 expression in vivo. The ges-1 GATA region was used as a probe to screen a C. elegans cDNA expression library, and a gene for a new C. elegans GATA-factor (named elt-2) was isolated. The longest open reading frame in the elt-2 cDNA codes for a protein of Mr 47,000 with a single zinc finger domain, similar (approximately 75% amino acid identity) to the C-terminal fingers of all other two-fingered GATA factors isolated to date. A similar degree of relatedness is found with the single-finger DNA binding domains of GATA factors identified in invertebrates. An upstream region in the ELT-2 protein with the sequence C-X2-C-XGraphic-C-X2-C has some of the characteristics of a zinc finger domain but is highly diverged from the zinc finger domains of other GATA factors. The elt-2 gene is expressed as an SL1 trans-spliced message, which can be detected at all stages of development except oocytes; however, elt-2 message levels are 5-10-fold higher in embryos than in other stages. The genomic clone for elt-2 has been characterized and mapped near the center of the C. elegans X chromosome. ELT-2 protein, produced by in vitro transcription-translation, binds to ges-1 GATA-containing oligonucleotides similar to a factor previously identified in C. elegans embryo extracts, both as assayed by electrophoretic migration and by competition with wild type and mutant oligonucleotides. However, there is as yet no direct evidence that elt-2 does or does not control ges-1.

Footnotes

  • * This work was supported by the Medical Research Council of Canada, the Alberta Heritage Foundation for Medical Research, the Science and Engineering Research Council of Great Britain (SERC), the North Atlantic Treaty Organization (NATO), and the Howard Hughes Medical Institute. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore by hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    The nucleotide sequence(s) reported in this paper has been submitted to the GenBankGraphic/EMBL Data Bank with accession number(s) U25175.

  • 1 The abbreviation used is:

    PCR

    polymerase chain reaction.

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