Sinclair D A, Clegg N J, Antonchuk J, Milne T A, Stankunas K, Ruse C, Grigliatti T A, Kassis J A, Brock H W
IMBB, Simon Fraser University, Burnaby, British Columbia, Canada.
Genetics. 1998 Jan;148(1):211-20. doi: 10.1093/genetics/148.1.211.
Polycomb group (PcG) genes of Drosophila are negative regulators of homeotic gene expression required for maintenance of determination. Sequence similarity between Polycomb and Su(var)205 led to the suggestion that PcG genes and modifiers of position-effect variegation (PEV) might function analogously in the establishment of chromatin structure. If PcG proteins participate directly in the same process that leads to PEV, PcG mutations should suppress PEV. We show that mutations in E(Pc), an unusual member of the PcG, suppress PEV of four variegating rearrangements: In(l)wm4, B(SV), T(2;3)Sb(V) and In(2R)bw(VDe2). Using reversion of a Pelement insertion, deficiency mapping, and recombination mapping as criteria, homeotic effects and suppression of PEV associated with E(Pc) co-map. Asx is an enhancer of PEV, whereas nine other PcG loci do not affect PEV. These results support the conclusion that there are fewer similarities between PcG genes and modifiers of PEV than previously supposed. However, E(Pc) appears to be an important link between the two groups. We discuss why Asx might act as an enhancer of PEV.
果蝇的多梳蛋白组(PcG)基因是维持细胞分化状态所需的同源异型基因表达的负调控因子。多梳蛋白与Su(var)205之间的序列相似性表明,PcG基因和位置效应斑驳(PEV)修饰因子可能在染色质结构的建立过程中发挥类似的作用。如果PcG蛋白直接参与导致PEV的相同过程,那么PcG突变应该会抑制PEV。我们发现,PcG中一个特殊成员E(Pc)的突变能够抑制四种斑驳重排的PEV:In(l)wm4、B(SV)、T(2;3)Sb(V)和In(2R)bw(VDe2)。以P因子插入的回复、缺失定位和重组定位为标准,与E(Pc)相关的同源异型效应和PEV抑制共定位。Asx是PEV的增强子,而其他九个PcG位点不影响PEV。这些结果支持了这样的结论,即PcG基因与PEV修饰因子之间的相似性比之前认为的要少。然而,E(Pc)似乎是这两组之间的一个重要联系。我们讨论了Asx为何可能作为PEV的增强子。