Functional Role of C-terminal Domains in the MSL2 Protein of Drosophila melanogaster

被引:1
|
作者
Tikhonova, Evgeniya A. [1 ]
Georgiev, Pavel G. [1 ]
Maksimenko, Oksana G. [1 ]
机构
[1] Russian Acad Sci, Inst Gene Biol, Moscow 119334, Russia
关键词
dosage compensation; long non-coding RNAs; MSL1; roX; MSL complex; ubiquitination; DOSAGE COMPENSATION COMPLEX; MALE-SPECIFIC LETHAL-2; SEX-SPECIFIC REGULATION; X-CHROMOSOME; RING FINGER; STRUCTURAL BASIS; CXC DOMAIN; GENE; BINDING; MOF;
D O I
10.1134/S0006297924040060
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dosage compensation complex (DCC), which consists of five proteins and two non-coding RNAs roX, specifically binds to the X chromosome in males, providing a higher level of gene expression necessary to compensate for the monosomy of the sex chromosome in male Drosophila compared to the two X chromosomes in females. The MSL2 protein contains the N-terminal RING domain, which acts as an E3 ligase in ubiquitination of proteins and is the only subunit of the complex expressed only in males. Functional role of the two C-terminal domains of the MSL2 protein, enriched with proline (P-domain) and basic amino acids (B-domain), was investigated. As a result, it was shown that the B-domain destabilizes the MSL2 protein, which is associated with the presence of two lysines ubiquitination of which is under control of the RING domain of MSL2. The unstructured proline-rich domain stimulates transcription of the roX2 gene, which is necessary for effective formation of the dosage compensation complex.
引用
收藏
页码:663 / 673
页数:11
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