Literature DB >> 1652526

An acid phosphatase as a biochemical marker for intestinal development in the nematode Caenorhabditis elegans.

C T Beh1, D C Ferrari, M A Chung, J D McGhee.   

Abstract

We describe an acid phosphatase enzyme (EC 3.1.3.2) that is localized to the intestine of the nematode Caenorhabditis elegans and that should serve as a convenient biochemical marker for gut differentiation. In adult worms, acid phosphatase activity is located along the edge of the gut lumen in the vicinity of the intestinal brush border. All but the anterior six cells of the intestine stain for phosphatase activity; the nonstaining cells all descend from the Ea(l/r)(a/p)a cells. Acid phosphatase activity is low in oocytes and early embryos but increases substantially when embryos reach late morphogenesis stage; this increase corresponds to the appearance of a major band of acid phosphatase activity detectable on isoelectric focusing gels. We designate this band as the product of the pho-1 gene. The pattern of acid phosphatase expression in several embryonic mutants suggests that pho-1 expression in the developing intestine is lineage autonomous. We induced an isoelectric focusing variant in the pho-1 enzyme and used this to map the pho-1 locus about 1.5 map units to the left of center of chromosome II. We purified the pho-1 enzyme to homogeneity (6500-fold purification; 4% recovery of activity); the pho-1 acid phosphatase is a homodimeric glycoprotein with a subunit molecular weight of 55,000 Da. This paper establishes a new experimental system with which to investigate the molecular basis of lineage-specific gene expression during C. elegans development.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1652526     DOI: 10.1016/s0012-1606(05)80013-2

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


  6 in total

1.  Cholinesterase and phosphatase activities in adults and infective-stage larvae of levamisole-resistant and levamisole-susceptible isolates of Haemonchus contortus.

Authors:  C Giménez-Pardo; M M Martínez-Grueiro; A Gómez-Barrio; F Rodríguez-Caabeiro
Journal:  Vet Res Commun       Date:  2003-12       Impact factor: 2.459

2.  Amelioration of metal-induced toxicity in Caenorhabditis elegans: utility of chelating agents in the bioremediation of metals.

Authors:  James M Harrington; Windy A Boyd; Marjolein V Smith; Julie R Rice; Jonathan H Freedman; Alvin L Crumbliss
Journal:  Toxicol Sci       Date:  2012-05-28       Impact factor: 4.849

3.  Endoderm development in Caenorhabditis elegans: the synergistic action of ELT-2 and -7 mediates the specification→differentiation transition.

Authors:  Erica M Sommermann; Keith R Strohmaier; Morris F Maduro; Joel H Rothman
Journal:  Dev Biol       Date:  2010-08-31       Impact factor: 3.582

4.  Revisiting histidine-dependent acid phosphatases: a distinct group of tyrosine phosphatases.

Authors:  Suresh Veeramani; Ming-Shyue Lee; Ming-Fong Lin
Journal:  Trends Biochem Sci       Date:  2009-05-19       Impact factor: 13.807

5.  In situ analysis of C. elegans vitellogenin fusion gene expression in integrated transgenic strains: effect of promoter mutations on RNA localization.

Authors:  M MacMorris; T Blumenthal
Journal:  Gene Expr       Date:  1993

6.  Imaging Cellular Inorganic Phosphate in Caenorhabditis elegans Using a Genetically Encoded FRET-Based Biosensor.

Authors:  Swayoma Banerjee; Wayne K Versaw; L Rene Garcia
Journal:  PLoS One       Date:  2015-10-20       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.