Source:http://linkedlifedata.com/resource/pubmed/id/17363251
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2007-4-4
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pubmed:abstractText |
X-linked signal elements (XSEs) communicate the dose of X chromosomes to the regulatory-switch gene Sex-lethal (Sxl) during Drosophila sex determination. Unequal XSE expression in precellular XX and XY nuclei ensures that only XX embryos will activate the establishment promoter, SxlPe, to produce a pulse of the RNA-binding protein, SXL [1]. Once XSE protein concentrations have been assessed, SxlPe is inactivated and the maintenance promoter, SxlPm, is turned on in both sexes; however, only in females is SXL present to direct the SxlPm-derived transcripts to be spliced into functional mRNA [2, 3]. Thereafter, Sxl is maintained in the on state by positive autoregulatory RNA splicing [2]. Once set in the stable on (female) or off (male) state, Sxl controls somatic sexual development through control of downstream effectors of sexual differentiation and dosage compensation [1, 4]. Most XSEs encode transcription factors that bind SxlPe, but the XSE unpaired (upd) encodes a secreted ligand for the JAK/STAT pathway [5-7]. We show that although STAT directly regulates SxlPe, it is dispensable for promoter activation. Instead, JAK/STAT is needed to maintain high-level SxlPe expression in order to ensure Sxl autoregulation in XX embryos. Thus, upd is a unique XSE that augments, rather than defines, the initial sex-determination signal.
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pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Janus Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/STAT Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Sxl protein, Drosophila,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/hopscotch protein, Drosophila,
http://linkedlifedata.com/resource/pubmed/chemical/os protein, Drosophila
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0960-9822
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
17
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
643-8
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:17363251-Animals,
pubmed-meshheading:17363251-Drosophila,
pubmed-meshheading:17363251-Drosophila Proteins,
pubmed-meshheading:17363251-Embryo, Nonmammalian,
pubmed-meshheading:17363251-Female,
pubmed-meshheading:17363251-Gene Expression Regulation, Developmental,
pubmed-meshheading:17363251-Janus Kinases,
pubmed-meshheading:17363251-Male,
pubmed-meshheading:17363251-RNA-Binding Proteins,
pubmed-meshheading:17363251-STAT Transcription Factors,
pubmed-meshheading:17363251-Sex Determination Processes,
pubmed-meshheading:17363251-Transcription, Genetic,
pubmed-meshheading:17363251-Transcription Factors,
pubmed-meshheading:17363251-X Chromosome
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pubmed:year |
2007
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pubmed:articleTitle |
Drosophila JAK/STAT pathway reveals distinct initiation and reinforcement steps in early transcription of Sxl.
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pubmed:affiliation |
Department of Biology, Texas A&M University, 3258 TAMU, College Station, TX 77843, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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