小基因
生物
RNA剪接
选择性拼接
外显子
蛋白质剪接
基因
遗传学
拼接因子
信使核糖核酸
蛋白质结构域
细胞生物学
分子生物学
核糖核酸
作者
Arisa Tanaka,Fugaku Aoki,Masataka G. Suzuki
摘要
The <i>transformer</i> (<i>tra</i>) gene, which is a female-determining master gene in the housefly <i>Musca domestica</i>, acts as a memory device for sex determination via its auto-regulatory function, i.e., through the contribution of the TRA protein to female-specific splicing of its own pre-mRNA. The TRA protein contains 4 small domains that are specifically conserved among TRA proteins (domains 1-4). Domain 2, also named TRA-CAM domain, is the most conserved, but its function remains unknown. To examine whether these domains are involved in the auto-regulatory function, we performed in vitro splicing assays using a <i>tra </i>minigene containing a partial genomic sequence of the <i>M. domestica tra</i> (<i>Mdtra</i>) gene. Co-transfection of the <i>Mdtra</i> minigene and an MdTRA protein expression vector into cultured insect cells strongly induced female-specific splicing of the minigene. A series of deletion mutation analyses demonstrated that these domains act complementarily to induce female-specific splicing. Domain 1 and the TRA-CAM domain were necessary for the female-specific splicing when the MdTRA protein lacked both domains 3 and 4. In this situation, mutation of the well-conserved 3 amino acids (GEG) in the TRA-CAM domain significantly reduced the female-specific splicing activity of MdTRA. GST-pull down analyses demonstrated that the MdTRA protein specifically enriched on the male-specific exonic region (exon 2b), which contains the putative TRA/TRA-2 binding sites, and that the GEG mutation disrupts this enrichment. Since the MdTRA protein interacts with its own pre-mRNA through TRA-2, our findings suggest that the conserved amino acid residues in the TRA-CAM domain may be crucial for the interaction between MdTRA and TRA-2, enhancing MdTRA recruitment on its pre-mRNA to induce female-specific splicing of<i> tra</i> in the housefly.
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