This proposal is a continuation of work designed to exploit the special features that Drosophila sex determination appears to offer for understanding how information for cellular differentiation in higher eukaryotes is genetically encoded, how it can be disrupted by mutations, and how it may have been evolved. The goal of this study is to understand the specific genetic regulatory mechanisms that operate in this organism to govern the initiation and maintenance of sex-specific pathways of development. The gene called Sex-lethal occupies a central position in this process. Tests of several hypotheses regarding Sxl's regulation are presented. One of the most important is the proposal that Sxl produces a positive self-regulatory product that is required for the initiation and/or maintenance of the gene's own activity state. Another is the proposal that a genetic element called sisterless-a is part of a system of elements whose overall relative dose serves as a developmental signal to determine Sxl's activity state very early in development. Only a 50% difference in this parameter elicits all the differences between the sexes. The genetic context in which Sxl operates will be explored, including genes that act in the mother to control, in an epigenetic fashion, the behavior of genes in the zygote. Temporal and tissue-specific aspects of Sxl's own regulation, and of its regulation of subordinate genes and/or gene products will be investigated. As a byproduct of this study of sex determination, a considerable amount should be learned regarding the effects of mobile genetic elements on gene function and meiotic recombination in higher eukaryotes. Many of the most useful mutant Sxl alleles carry insertions and rearrangements of such mobile elements. This analysis will be carried out using the techniques of developmental genetics which have proven so powerful over the past eight years of this study. This genetic work will complement a parallel study of Sxl at the molecular level, a study that was made possible by the genetic analysis that preceded it. Information from the experiments proposed here should provide the background needed to extend molecular analysis of this system into important new areas.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM023468-09A1
Application #
3271654
Study Section
Genetics Study Section (GEN)
Project Start
1977-01-01
Project End
1990-11-30
Budget Start
1985-12-01
Budget End
1986-11-30
Support Year
9
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Princeton University
Department
Type
Schools of Arts and Sciences
DUNS #
002484665
City
Princeton
State
NJ
Country
United States
Zip Code
08544
Evans, Daniel S; Cline, Thomas W (2013) Drosophila switch gene Sex-lethal can bypass its switch-gene target transformer to regulate aspects of female behavior. Proc Natl Acad Sci U S A 110:E4474-81
Cline, Thomas W; Dorsett, Maia; Sun, Sha et al. (2010) Evolution of the Drosophila feminizing switch gene Sex-lethal. Genetics 186:1321-36
Harrison, Melissa M; Botchan, Michael R; Cline, Thomas W (2010) Grainyhead and Zelda compete for binding to the promoters of the earliest-expressed Drosophila genes. Dev Biol 345:248-55
Sun, Sha; Cline, Thomas W (2009) Effects of Wolbachia infection and ovarian tumor mutations on Sex-lethal germline functioning in Drosophila. Genetics 181:1291-301
Siera, Scott G; Cline, Thomas W (2008) Sexual back talk with evolutionary implications: stimulation of the Drosophila sex-determination gene sex-lethal by its target transformer. Genetics 180:1963-81
Evans, Daniel S; Cline, Thomas W (2007) Drosophila melanogaster male somatic cells feminized solely by TraF can collaborate with female germ cells to make functional eggs. Genetics 175:631-42
ten Bosch, John R; Benavides, Joseph A; Cline, Thomas W (2006) The TAGteam DNA motif controls the timing of Drosophila pre-blastoderm transcription. Development 133:1967-77
Wrischnik, Lisa A; Timmer, John R; Megna, Lisa A et al. (2003) Recruitment of the proneural gene scute to the Drosophila sex-determination pathway. Genetics 165:2007-27
Cline, T W; Rudner, D Z; Barbash, D A et al. (1999) Functioning of the Drosophila integral U1/U2 protein Snf independent of U1 and U2 small nuclear ribonucleoprotein particles is revealed by snf(+) gene dose effects. Proc Natl Acad Sci U S A 96:14451-8
Erickson, J W; Cline, T W (1998) Key aspects of the primary sex determination mechanism are conserved across the genus Drosophila. Development 125:3259-68

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