Dominado Nicole, Ye Rachel, Casagranda Franca, Heaney James, Siddall Nicole A, Abud Helen E, Hime Gary R
Department of Anatomy and Physiology, University of Melbourne, Parkville, VIC, Australia.
Department of Anatomy and Developmental Biology, Biomedicine Discovery Institute, Monash University, Clayton, VIC, Australia.
Cell Death Discov. 2025 Apr 29;11(1):206. doi: 10.1038/s41420-025-02496-8.
Regeneration of the Drosophila midgut epithelium depends upon differential expression of transcription factors in intestinal stem cells and their progeny. The grainy head locus produces multiple splice forms that result in production of two classes of transcription factor, designated Grh.O and Grh.N. grainy head expression is associated with epithelial tissue and has roles in epidermal development and regeneration but had not been examined for a function in the midgut epithelium. Here we show that null mutant clones had a limited effect on intestinal stem cell (ISC) maintenance and proliferation but surprisingly specific loss of all Grh.O isoforms results in loss of ISCs from the epithelium. This was confirmed by generation of a new Grh.O class mutant to control for genetic background effects. Grh.O mutant ISCs were not lost due to cell death but were forced to differentiate. Ectopic expression of a Grh.N isoform also resulted in ISC differentiation similar to loss of Grh.O function. Grh.O expression must be tightly regulated as high level ectopic expression of a member of this isoform class in enteroblasts, but not ISCs, resulted in cells with confused identity and promoted excess proliferation in the epithelium. Thus, midgut regeneration is not only dependent upon signalling pathways that regulate transcription factor expression, but also upon regulated mRNA splicing of these genes.
果蝇中肠上皮的再生取决于肠道干细胞及其后代中转录因子的差异表达。颗粒头基因座产生多种剪接形式,导致产生两类转录因子,分别命名为Grh.O和Grh.N。颗粒头的表达与上皮组织相关,在表皮发育和再生中发挥作用,但尚未研究其在中肠上皮中的功能。在这里,我们表明,无效突变克隆对肠道干细胞(ISC)的维持和增殖影响有限,但令人惊讶的是,所有Grh.O异构体的特异性缺失导致上皮中ISC的丧失。通过产生一种新的Grh.O类突变体来控制遗传背景效应,这一点得到了证实。Grh.O突变体ISC并非因细胞死亡而丧失,而是被迫分化。Grh.N异构体的异位表达也导致ISC分化,类似于Grh.O功能丧失。Grh.O的表达必须受到严格调控,因为该异构体类成员在成肠细胞而非ISC中的高水平异位表达会导致细胞身份混乱,并促进上皮中的过度增殖。因此,中肠再生不仅取决于调节转录因子表达的信号通路,还取决于这些基因的mRNA剪接调控。