Bashirullah Arash, Lam Geanette, Yin Viravuth P, Thummel Carl S
Department of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah 84112-5330, USA.
Dev Dyn. 2007 Nov;236(11):3173-9. doi: 10.1002/dvdy.21350.
The TATA box-binding protein (TBP) related factor 2 (TRF2) has been well characterized at a biochemical level and in cultured cells. Relatively little, however, is known about how TRF2 functions in specific biological pathways during development. Here, we show that Drosophila TRF2 (dTRF2) plays an essential role in responses to the steroid hormone ecdysone during the onset of metamorphosis. Hypomorphic dTrf2 mutations lead to developmental arrest during prepupal and early pupal stages with defects in major ecdysone-triggered biological responses, including puparium formation, anterior spiracle eversion, gas bubble translocation, adult head eversion, and larval salivary gland cell death. The transcription of key ecdysone-regulated target genes is delayed and reduced in dTrf2 mutants. dTrf2 appears to be required for the proper timing and levels of ecdysone-regulated gene expression required for entry into metamorphosis.
TATA 盒结合蛋白(TBP)相关因子 2(TRF2)已在生化水平和培养细胞中得到充分表征。然而,对于 TRF2 在发育过程中如何在特定生物学途径中发挥作用,人们了解得相对较少。在这里,我们表明果蝇 TRF2(dTRF2)在变态开始期间对类固醇激素蜕皮激素的反应中起重要作用。低表达的 dTrf2 突变导致在蛹前期和早期蛹期发育停滞,主要蜕皮激素触发的生物学反应出现缺陷,包括蛹壳形成、前气门外翻、气泡移位、成虫头部外翻和幼虫唾液腺细胞死亡。dTrf2 突变体中关键蜕皮激素调节的靶基因转录延迟且减少。dTrf2 似乎是进入变态所需的蜕皮激素调节基因表达的正确时间和水平所必需的。