Gutjahr T, Frei E, Spicer C, Baumgartner S, White R A, Noll M
Institute for Molecular Biology, University of Zürich, Switzerland, UK.
EMBO J. 1995 Sep 1;14(17):4296-306. doi: 10.1002/j.1460-2075.1995.tb00104.x.
We have delimited the extra sex combs (esc) gene to < 4 kb that include a single transcript and are able to rescue both the maternal and zygotic esc phenotypes. Several mutations have been identified within the esc transcript. In agreement with earlier genetic studies, esc is expressed maternally and its product is most abundant during the early embryonic stages. It encodes a protein of the WD-40 repeat family, which localizes predominantly to the nucleus. During germ band extension, it is expressed in a stereotypic pattern of neuroblasts. We propose a model in which Esc is recruited by gap proteins both to act as a corepressor that competes with the TAFII80 coactivator to block transcription and also to mediate the transition to permanent repression by Polycomb-group proteins.
我们已将额外性梳(esc)基因定位到小于4 kb的区域,该区域包含单一转录本,并且能够挽救母体和合子esc表型。在esc转录本中已鉴定出多个突变。与早期的遗传学研究一致,esc在母体中表达,其产物在胚胎早期最为丰富。它编码一种WD-40重复家族的蛋白质,主要定位于细胞核。在胚带延伸期间,它以神经母细胞的定型模式表达。我们提出了一个模型,其中Esc被间隙蛋白招募,既作为与TAFII80共激活因子竞争以阻断转录的共抑制因子,又介导由多梳蛋白介导的向永久抑制的转变。