Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1993-4-6
pubmed:abstractText
The ges-1 gene codes for a non-specific carboxylesterase that is normally expressed only in the intestine of the nematode Caenorhabditis elegans. In the current paper, we describe the cloning and characterization of the ges-1 gene from C. elegans, as well as the homologous gene from the nematode Caenorhabditis briggsae. The ges-1 esterases from the two nematodes are 83% identical at the amino acid level and contain regions of significant similarity to insect and mammalian esterases; these conserved regions can be identified with residues believed to be necessary for esterase function. The ges-1 mRNAs from both C. elegans and C. briggsae are trans-spliced. The coding regions, the codon bias and the splicing signals of the two ges-1 genes are quite similar and most (6/7) of the intron positions are retained precisely. Yet, the flanking sequences of the two ges-1 genes appear to have diverged almost completely. For example, the C. elegans ges-1 5'-flanking region (as well as several introns) contains copies of three different SINE-like sequences, previously identified near the hsp-16 genes, near the unc-22 gene and in a repetitive element CeRep-3; none of these elements are found in the C. briggsae ges-1 gene. We show that: (1) the C. elegans ges-1 gene can be used to transform C. briggsae, whereupon expression of the exogenous ges-1 gene is confined to the C. briggsae intestine; (2) the ges-1 homologue cloned from C. briggsae can be transformed into C. elegans, whereupon it is expressed largely in the C. elegans intestine; and (3) a 5'-deletion of the C. elegans ges-1 gene that we have previously shown to be expressed in the C. elegans pharynx is also expressed in the pharynx of C. briggsae (either in the presence or absence of vector sequences). These results suggest that the ges-1 gene control circuits have been maintained between the two nematode species, despite the divergent 5'-flanking sequences of the gene. This raises the question of the evolutionary distance between C. elegans and C. briggsae and we attempt to estimate the C. elegans-C. briggsae divergence time by analysing the rate of synonymous substitutions in coding regions of ges-1 and six other C. elegans-C. briggsae gene pairs. We propose a new method of analysis, which attempts to remove rate differences found between different genes by extrapolating to zero codon bias.(ABSTRACT TRUNCATED AT 400 WORDS)
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0022-2836
pubmed:author
pubmed:issnType
Print
pubmed:day
20
pubmed:volume
229
pubmed:geneSymbol
ges-1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
890-908
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:8445654-Amino Acid Sequence, pubmed-meshheading:8445654-Animals, pubmed-meshheading:8445654-Base Sequence, pubmed-meshheading:8445654-Biological Evolution, pubmed-meshheading:8445654-Caenorhabditis, pubmed-meshheading:8445654-Caenorhabditis elegans, pubmed-meshheading:8445654-Caenorhabditis elegans Proteins, pubmed-meshheading:8445654-Carboxylic Ester Hydrolases, pubmed-meshheading:8445654-Cloning, Molecular, pubmed-meshheading:8445654-DNA, pubmed-meshheading:8445654-Digestive System, pubmed-meshheading:8445654-Gene Expression Regulation, Enzymologic, pubmed-meshheading:8445654-Gene Library, pubmed-meshheading:8445654-Genetic Variation, pubmed-meshheading:8445654-Molecular Sequence Data, pubmed-meshheading:8445654-Repetitive Sequences, Nucleic Acid, pubmed-meshheading:8445654-Restriction Mapping, pubmed-meshheading:8445654-Sequence Homology, Nucleic Acid, pubmed-meshheading:8445654-Transformation, Genetic
pubmed:year
1993
pubmed:articleTitle
The gut esterase gene (ges-1) from the nematodes Caenorhabditis elegans and Caenorhabditis briggsae.
pubmed:affiliation
Department of Medical Biochemistry, University of Calgary, Alberta, Canada.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't