Mollaaghababa R, Sipos L, Tiong S Y, Papoulas O, Armstrong J A, Tamkun J W, Bender W
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):3958-63. doi: 10.1073/pnas.061497798.
The homeotic genes controlling segment identity in Drosophila are repressed by the Polycomb group of genes (PcG) and are activated by genes of the trithorax group (trxG). An F(1) screen for dominant enhancers of Polycomb yielded a point mutation in the heat shock cognate gene, hsc4, along with mutations corresponding to several known PcG loci. The new mutation is a more potent enhancer of Polycomb phenotypes than an apparent null allele of hsc4 is, although even the null allele occasionally displays homeotic phenotypes associated with the PcG. Previous biochemical results had suggested that HSC4 might interact with BRAHMA, a trxG member. Further analyses now show that there is no physical or genetic interaction between HSC4 and the Brahma complex. HSC4 might be needed for the proper folding of a component of the Polycomb repression complex, or it may be a functional member of that complex.
控制果蝇体节特征的同源异型基因受到多梳基因家族(PcG)的抑制,并被三胸节基因家族(trxG)的基因激活。一项针对多梳显性增强子的F(1)筛选在热休克同源基因hsc4中产生了一个点突变,同时还产生了与几个已知PcG位点相对应的突变。这个新突变比hsc4的一个明显的无效等位基因是更强效的多梳表型增强子,尽管即使是无效等位基因偶尔也会表现出与PcG相关的同源异型表型。先前的生化结果表明,HSC4可能与trxG成员BRAHMA相互作用。现在的进一步分析表明,HSC4与Brahma复合体之间不存在物理或遗传相互作用。HSC4可能是多梳抑制复合体一个组分正确折叠所必需的,或者它可能是该复合体的一个功能成员。