Sex lethal controls dosage compensation in Drosophila by a non-splicing mechanism

被引:215
作者
Kelley, RL
Wang, JW
Bell, L
Kuroda, MI
机构
[1] BAYLOR COLL MED,DEPT CELL BIOL,HOUSTON,TX 77030
[2] BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
[3] UNIV SO CALIF,PROGRAM MOL BIOL,LOS ANGELES,CA 90089
关键词
X-CHROMOSOME; TRANSLATIONAL REGULATION; MESSENGER-RNAS; GENE; BINDING; INITIATION; PROTEIN; MELANOGASTER; EXPRESSION; ENCODES;
D O I
10.1038/387195a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Dosage compensation in Drosophila requires the male-specific lethal (msl) proteins (MSL) to make gene expression from the single male X chromosome equivalent to that from both female X chromosomes(1,2). Expression of msl2 is repressed post-transcriptionally by Sex lethal (SXL), a female-specific RNA-binding protein that regulates alternative splicing in the sex-determination hierarchy, Although msl2 RNA is alternatively spliced in males and females, this does not alter its coding potential and splicing is not required for male-specific expression of MSL2 protein. Instead, our results suggest that the association of SXL protein with multiple sites in the 5' and 3' untranslated regions of the mxl2 transcript represses its translation in females. Thus, this well characterized alternative splicing factor regulates at least one target transcript by a distinct mechanism.
引用
收藏
页码:195 / 199
页数:5
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