This research addresses the question of how the genes of a multicellular organism specify the development and final form of the organism. This question is addressed by focusing on the genetic basis of the development of a specific, well-defined, dispensible structure in the soil roundworm Caenorhabditis elegans. The structure that will be studied in the copulatory organ of the adult male tail. This structure comprises 164 male- specific cells that arise by post-embryonic divisions of 12 precursor cells. Genes will be identified that determine both the production of the male tail-specific cells and the coordinated differentiation of those cells into the final adult structure. Genes will be identified by isolating mutants with abnormal male tails (mab mutants). Mutant isolation will be accomplished by screening mutagenized cultures with the dissecting microscope. Mutations will be placed into complementation groups and mapped with respect to known genes. Mutant phenotypes will be analyzed in detail with the compound microscope. Mutations are especially sought that affect a particular set of easily-observed sublineages within the tail. These sublineages are responsible for producing repetitive structures called rays. Electron microscopic, immunocytochemical, and laser ablation techniques will be used to determine whether another prominent structure, the fan, is also a product of these sublineages. Mutations that affect the fan and rays will be analyzed at the level of cell lineage.
The aim i s to identify genes that specify cell fates in the ray sublineages. Basic studies of normal development in accessible model systems, such as those described here, will aid in the understanding of disrupted processes in developmental and neoplastic diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM039353-03
Application #
3296257
Study Section
Genetics Study Section (GEN)
Project Start
1988-02-01
Project End
1992-01-31
Budget Start
1990-02-01
Budget End
1992-01-31
Support Year
3
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
Schools of Medicine
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
Emmons, Scott W (2016) Connectomics, the Final Frontier. Curr Top Dev Biol 116:315-30
Zhang, Hongjie; Emmons, Scott W (2009) Regulation of the Caenorhabditis elegans posterior Hox gene egl-5 by microRNA and the polycomb-like gene sop-2. Dev Dyn 238:595-603
Jia, Lingyun; Emmons, Scott W (2006) Genes that control ray sensory neuron axon development in the Caenorhabditis elegans male. Genetics 173:1241-58
Teng, Yingqi; Girard, Lisa; Ferreira, Henrique B et al. (2004) Dissection of cis-regulatory elements in the C. elegans Hox gene egl-5 promoter. Dev Biol 276:476-92
Toker, Anne S; Teng, Yingqi; Ferreira, Henrique B et al. (2003) The Caenorhabditis elegans spalt-like gene sem-4 restricts touch cell fate by repressing the selector Hox gene egl-5 and the effector gene mec-3. Development 130:3831-40
Zhang, Hong; Azevedo, Ricardo B R; Lints, Robyn et al. (2003) Global regulation of Hox gene expression in C. elegans by a SAM domain protein. Dev Cell 4:903-15
Hahn, Andrew C; Emmons, Scott W (2003) The roles of an ephrin and a semaphorin in patterning cell-cell contacts in C. elegans sensory organ development. Dev Biol 256:379-88
Zhang, Hong; Emmons, Scott W (2002) Caenorhabditis elegans unc-37/groucho interacts genetically with components of the transcriptional mediator complex. Genetics 160:799-803
Zhang, H; Emmons, S W (2001) The novel C. elegans gene sop-3 modulates Wnt signaling to regulate Hox gene expression. Development 128:767-77
Zhang, H; Emmons, S W (2000) A C. elegans mediator protein confers regulatory selectivity on lineage-specific expression of a transcription factor gene. Genes Dev 14:2161-72

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