Literature DB >> 3956859

Embryonic expression of a gut-specific esterase in Caenorhabditis elegans.

L G Edgar, J D McGhee.   

Abstract

We describe an esterase activity that, by the criterion of histochemical staining, is completely localized to the intestine of the nematode Caenorhabditis elegans. Esterase activity appears in the embryonic gut when the embryo contains 4-8 intestinal precursor cells and 100-150 total cells. Esterase activity is abolished by treating early embryos with alpha-amanitin, indicating that expression depends upon transcription by RNA polymerase II within the developing embryo. In partial embryos produced by lysing one blastomere of a two-cell embryo, esterase expression appears only in descendants of the blastomere that normally produces the gut; esterase expression appears independent of the other non-gut blastomere. In early cleavage-stage embryos in which cytokinesis has been blocked by cytochalasin D, esterase expression appears at the normal time and only in cells in the gut lineage; thus neither normal cell division nor normal embryogenesis is required for lineage-specific expression. However, esterase does not appear in cytochalasin D blocked one-cell embryos. These observations confirm the traditional view that C. elegans development is "mosaic," with each cell following a defined independent program of gene expression.

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Year:  1986        PMID: 3956859     DOI: 10.1016/0012-1606(86)90387-8

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  26 in total

1.  Dominant maternal-effect mutations causing embryonic lethality in Caenorhabditis elegans.

Authors:  P E Mains; I A Sulston; W B Wood
Journal:  Genetics       Date:  1990-06       Impact factor: 4.562

2.  Reprogramming of early embryonic blastomeres into endodermal progenitors by a Caenorhabditis elegans GATA factor.

Authors:  J Zhu; T Fukushige; J D McGhee; J H Rothman
Journal:  Genes Dev       Date:  1998-12-15       Impact factor: 11.361

3.  ADM-1, a protein with metalloprotease- and disintegrin-like domains, is expressed in syncytial organs, sperm, and sheath cells of sensory organs in Caenorhabditis elegans.

Authors:  B Podbilewicz
Journal:  Mol Biol Cell       Date:  1996-12       Impact factor: 4.138

4.  Genes that implement the hermaphrodite mode of dosage compensation in Caenorhabditis elegans.

Authors:  J D Plenefisch; L DeLong; B J Meyer
Journal:  Genetics       Date:  1989-01       Impact factor: 4.562

5.  Reevaluation of the role of the med-1 and med-2 genes in specifying the Caenorhabditis elegans endoderm.

Authors:  Barbara Goszczynski; James D McGhee
Journal:  Genetics       Date:  2005-07-05       Impact factor: 4.562

6.  TRX-1 Regulates SKN-1 Nuclear Localization Cell Non-autonomously in Caenorhabditis elegans.

Authors:  Katie C McCallum; Bin Liu; Juan Carlos Fierro-González; Peter Swoboda; Swathi Arur; Antonio Miranda-Vizuete; Danielle A Garsin
Journal:  Genetics       Date:  2016-02-26       Impact factor: 4.562

7.  Quantitating transcription factor redundancy: The relative roles of the ELT-2 and ELT-7 GATA factors in the C. elegans endoderm.

Authors:  Aidan Dineen; Erin Osborne Nishimura; Barbara Goszczynski; Joel H Rothman; James D McGhee
Journal:  Dev Biol       Date:  2018-01-31       Impact factor: 3.582

8.  The major gut esterase locus in the nematode Caenorhabditis elegans.

Authors:  J D McGhee; D A Cottrell
Journal:  Mol Gen Genet       Date:  1986-01

9.  P-type ATPase TAT-2 negatively regulates monomethyl branched-chain fatty acid mediated function in post-embryonic growth and development in C. elegans.

Authors:  Emylie Seamen; Jennifer M Blanchette; Min Han
Journal:  PLoS Genet       Date:  2009-08-07       Impact factor: 5.917

10.  The evolutionary duplication and probable demise of an endodermal GATA factor in Caenorhabditis elegans.

Authors:  Tetsunari Fukushige; Barbara Goszczynski; Helen Tian; James D McGhee
Journal:  Genetics       Date:  2003-10       Impact factor: 4.562

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