Eberl D F, Lorenz L J, Melnick M B, Sood V, Lasko P, Perrimon N
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115, USA.
Genetics. 1997 Jul;146(3):951-63. doi: 10.1093/genetics/146.3.951.
In Drosophila melanogaster, position-effect variegation of the white gene has been a useful phenomenon by which to study chromosome structure and the genes that modify it. We have identified a new enhancer of variegation locus, Dmrnahel (hel). Deletion of mutation of hel enhances white variegation, and this can be reversed by a transformed copy of hel+. In the presence of two endogenous copies, the transformed hel+ behaves as a suppressor of variegation. hel is an essential gene and functions both maternally and zygotically. The HEL protein is similar to known RNA helicases, but contains an unusual variant (DECD) of the DEAD motif common to these proteins. Potential HEL homologues have been found in mammals, yeast and worms. HEL protein associates with salivary gland chromosomes and locates to nuclei of embryos and ovaries, but disappears in mitotic domains of embryos as chromosomes condense. We propose that the HEL protein promotes an open chromatin structure that favors transcription during development by regulating the spread of heterochromatin, and that HEL is regulated by, and may have a role in, the mitotic cell cycle during embryogenesis.
在黑腹果蝇中,白色基因的位置效应斑驳一直是研究染色体结构及其修饰基因的有用现象。我们鉴定出了一个新的斑驳位点增强子,即Dmrnahel(hel)。hel的缺失突变会增强白色基因的斑驳现象,而导入hel+的转化拷贝可以使其逆转。在存在两个内源拷贝的情况下,转化后的hel+表现为斑驳现象的抑制因子。hel是一个必需基因,在母体和合子中均发挥作用。HEL蛋白与已知的RNA解旋酶相似,但含有这些蛋白共有的DEAD基序的一个不寻常变体(DECD)。在哺乳动物、酵母和蠕虫中已发现潜在的HEL同源物。HEL蛋白与唾液腺染色体结合,并定位于胚胎和卵巢的细胞核中,但在胚胎的有丝分裂区域中,随着染色体浓缩而消失。我们推测,HEL蛋白通过调节异染色质的扩散来促进一种有利于发育过程中转录的开放染色质结构,并且HEL在胚胎发生过程中受有丝分裂细胞周期的调控,可能在其中发挥作用。