Andrews J, Garcia-Estefania D, Delon I, Lü J, Mével-Ninio M, Spierer A, Payre F, Pauli D, Oliver B
Laboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda MD, USA.
Development. 2000 Feb;127(4):881-92. doi: 10.1242/dev.127.4.881.
OVO controls germline and epidermis differentiation in flies and mice. In the Drosophila germline, alternative OVO-B and OVO-A isoforms have a common DNA-binding domain, but different N-termini. We show that these isoforms are transcription factors with opposite regulatory activities. Using yeast one-hybrid assays, we identified a strong activation domain within a common region and a counteracting repression domain within the OVO-A-specific region. In flies, OVO-B positively regulated the ovarian tumor promoter, while OVO-A was a negative regulator of the ovarian tumor and ovo promoters. OVO-B isoforms supplied ovo(+) function in the female germline and epidermis, while OVO-A isoforms had dominant-negative activity in both tissues. Moreover, elevated expression of OVO-A resulted in maternal-effect lethality while the absence of OVO-A resulted in maternal-effect sterility. Our data indicate that tight regulation of antagonistic OVO-B and OVO-A isoforms is critical for germline formation and differentiation.
OVO调控果蝇和小鼠生殖系及表皮的分化。在果蝇生殖系中,选择性的OVO - B和OVO - A异构体具有共同的DNA结合结构域,但N端不同。我们发现这些异构体是具有相反调控活性的转录因子。通过酵母单杂交试验,我们在共同区域内鉴定出一个强激活结构域,在OVO - A特异性区域内鉴定出一个起抵消作用的抑制结构域。在果蝇中,OVO - B正向调控卵巢肿瘤启动子,而OVO - A是卵巢肿瘤和ovo启动子的负调控因子。OVO - B异构体在雌性生殖系和表皮中提供ovo(+)功能,而OVO - A异构体在这两个组织中具有显性负性活性。此外,OVO - A的表达升高导致母性效应致死,而缺乏OVO - A则导致母性效应不育。我们的数据表明,对拮抗的OVO - B和OVO - A异构体进行严格调控对于生殖系的形成和分化至关重要。