The overall goal of the proposed research is to extend the genetic analysis of the development of the free-living nematode Caenorhabditis elegans, a model organism for studying the genetic basis of animal development and behavior, chosen because of its limited size and cell number, its rigidly specified development, and its suitability for genetic manipulation. An understanding of the genetic basis of development may well be fundamental to much of medicine and may ultimately contribute important information to many problems, ranging from congenital defects to senescence. More specific objectives are: first, to continue the analysis of genetic mosaics produced by the somatic loss of free chromosome fragments in order to localize the anatomical foci of action of various genes known to affect animal behavior, development or anatomy; second, to identify and characterize gynandromorphs in which some cells are XX (normally hermaphrodite) and other cells are XO (normally male); third, to identify and characterize new chromosome duplications, both free and translocated and both X duplications and autosomal duplications, which will be used both to balance recessive lethal and sterile mutations and to generate genetic mosaics; fourth, to tag several genes that affect nervous system development with the transposon Tc1 and to make use of the Tc1 tag to clone at least one of these genes; and fifth, to continue manufacturing, in addition to chromosome duplications, rearranged chromosomes that can act as dominant crossover suppressors, which can be used to balance recessive lethal and sterile mutations.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM022387-13
Application #
3271119
Study Section
Genetics Study Section (GEN)
Project Start
1979-03-01
Project End
1992-02-29
Budget Start
1988-03-01
Budget End
1989-02-28
Support Year
13
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Type
Schools of Arts and Sciences
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Yochem, John; Lažeti?, Vladimir; Bell, Leslie et al. (2015) C. elegans NIMA-related kinases NEKL-2 and NEKL-3 are required for the completion of molting. Dev Biol 398:255-66
Bell, Leslie R; Stone, Steven; Yochem, John et al. (2006) The molecular identities of the Caenorhabditis elegans intraflagellar transport genes dyf-6, daf-10 and osm-1. Genetics 173:1275-86
Yochem, John; Hall, David H; Bell, Leslie R et al. (2005) Isopentenyl-diphosphate isomerase is essential for viability of Caenorhabditis elegans. Mol Genet Genomics 273:158-66
Spartz, Angela K; Herman, Robert K; Shaw, Jocelyn E (2004) SMU-2 and SMU-1, Caenorhabditis elegans homologs of mammalian spliceosome-associated proteins RED and fSAP57, work together to affect splice site choice. Mol Cell Biol 24:6811-23
Yochem, John; Bell, Leslie R; Herman, Robert K (2004) The identities of sym-2, sym-3 and sym-4, three genes that are synthetically lethal with mec-8 in Caenorhabditis elegans. Genetics 168:1293-306
Spike, Caroline A; Davies, Andrew G; Shaw, Jocelyn E et al. (2002) MEC-8 regulates alternative splicing of unc-52 transcripts in C. elegans hypodermal cells. Development 129:4999-5008
Spike, C A; Shaw, J E; Herman, R K (2001) Analysis of smu-1, a gene that regulates the alternative splicing of unc-52 pre-mRNA in Caenorhabditis elegans. Mol Cell Biol 21:4985-95
Davies, A G; Spike, C A; Shaw, J E et al. (1999) Functional overlap between the mec-8 gene and five sym genes in Caenorhabditis elegans. Genetics 153:117-34
Herman, M A; Ch'ng, Q; Hettenbach, S M et al. (1999) EGL-27 is similar to a metastasis-associated factor and controls cell polarity and cell migration in C. elegans. Development 126:1055-64
Lundquist, E A; Herman, R K; Shaw, J E et al. (1998) UNC-115, a conserved protein with predicted LIM and actin-binding domains, mediates axon guidance in C. elegans. Neuron 21:385-92

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