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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1985-9-16
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pubmed:abstractText |
Revertants of unc-15(e73)I, a paralyzed mutant with an altered muscle paramyosin, include six dominant and two recessive intragenic unc-15 revertants, two new alleles of the previously identified suppressor gene, sup-3 V, and a new suppressor designated sup-19(m210)V. The recessive intragenic unc-15 revertants exhibit novel alterations in paramyosin paracrystal structure and distribution, and these alterations are modified by interaction with unc-82(e1220)IV, another mutation that affects paramyosin. A strain containing both unc-15 and a mutation in sup-3 V that restores movement was mutagenized, and paralyzed mutants resembling unc-15 were isolated. Twenty mutations that interfere with suppression were divided into three classes (nonmuscle, sus-1, and mutations within sup-3) based on phenotype, genetic map position and dominance. The nonmuscle mutations include dumpy and uncoordinated types that have no obvious direct effect on muscle organization. Two recessive mutations define a new gene, sus-1 III. These mutations modify the unc-15(e73) phenotype to produce a severely paralyzed, dystrophic double mutant that is not suppressed by sup-3. Five semidominant, intragenic sup-3 antisuppressor mutations, one of which occurred spontaneously, restore the wild-type sup-3 phenotype of nonsuppression. However, reversion of these mutants generated no new suppressor alleles of sup-3, suggesting that the sup-3 antisuppressor alleles are not wild type but may be null alleles.
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pubmed:grant | |
pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/4018568-6352051,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4018568-6378619,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4018568-6894129,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4018568-7190524,
http://linkedlifedata.com/resource/pubmed/commentcorrection/4018568-7348600
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0016-6731
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
110
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
421-40
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:4018568-Animals,
pubmed-meshheading:4018568-Caenorhabditis,
pubmed-meshheading:4018568-Diethylstilbestrol,
pubmed-meshheading:4018568-Ethyl Methanesulfonate,
pubmed-meshheading:4018568-Formaldehyde,
pubmed-meshheading:4018568-Genes,
pubmed-meshheading:4018568-Genetic Linkage,
pubmed-meshheading:4018568-Genotype,
pubmed-meshheading:4018568-Heterozygote,
pubmed-meshheading:4018568-Muscles,
pubmed-meshheading:4018568-Mutation,
pubmed-meshheading:4018568-Suppression, Genetic,
pubmed-meshheading:4018568-Tropomyosin
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pubmed:year |
1985
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pubmed:articleTitle |
Gene interactions affecting muscle organization in Caenorhabditis elegans.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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