A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Spierer, A., Begeot, F., Spierer, P., Delattre, M. (2008). SU(VAR)3-7 links heterochromatin and dosage compensation in Drosophila.  PLoS Genet. 4(5): e1000066. (Export to RIS)
FlyBase ID FBrf0210330
Publication Type Research paper
PubMed ID 18451980
PubMed Abstract In Drosophila, dosage compensation augments X chromosome-linked transcription in males relative to females. This process is achieved by the Dosage Compensation Complex (DCC), which associates specifically with the male X chromosome. We previously found that the morphology of this chromosome is sensitive to the amounts of the heterochromatin-associated protein SU(VAR)3-7. In this study, we examine the impact of change in levels of SU(VAR)3-7 on dosage compensation. We first demonstrate that the DCC makes the X chromosome a preferential target for heterochromatic markers. In addition, reduced or increased amounts of SU(VAR)3-7 result in redistribution of the DCC proteins MSL1 and MSL2, and of Histone 4 acetylation of lysine 16, indicating that a wild-type dose of SU(VAR)3-7 is required for X-restricted DCC targeting. SU(VAR)3-7 is also involved in the dosage compensated expression of the X-linked white gene. Finally, we show that absence of maternally provided SU(VAR)3-7 renders dosage compensation toxic in males, and that global amounts of heterochromatin affect viability of ectopic MSL2-expressing females. Taken together, these results bring to light a link between heterochromatin and dosage compensation.
DOI 10.1371/journal.pgen.1000066
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Language of Publication English
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Publication Type Journal
Abbreviation PLoS Genet.
Title PLoS Genetics
Publication Year 2005-
ISBN/ISSN 1553-7404 1553-7390
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