DiBello P R, Withers D A, Bayer C A, Fristrom J W, Guild G M
Department of Biology, University of Pennsylvania, Philadelphia 19104-6018.
Genetics. 1991 Oct;129(2):385-97. doi: 10.1093/genetics/129.2.385.
The Broad-Complex (BR-C) is essential for metamorphosis in Drosophila melanogaster. This locus is coextensive with the 2B5 ecdysone-responsive early puff and is necessary for puffing and transcription of many subsequently activated late genes in the developing salivary gland. Mapping of 31 cDNA clones indicates that approximately 100 kb of the genome is devoted to the synthesis of many BR-C RNAs. Sequence analyses of these cDNA clones show that the BR-C encodes a family of related proteins characterized by a common core amino-terminal domain fused to alternate carboxy domains each containing a pair of zinc fingers. Most proteins also contain domains rich in distinctive amino acids located between the common core and zinc finger regions. BR-C mutant alleles resulting from chromosomal rearrangements at 2B5 are associated with deletions of 5'-untranslated sequences, separation of the core coding domain from the downstream zinc finger domains, or a P element insertional disruption of a zinc finger coding sequence. We infer that the BR-C directly regulates late gene expression by specifying the synthesis of a family of proteins with DNA binding potential.
泛复合体(BR-C)对于黑腹果蝇的变态发育至关重要。该基因座与2B5蜕皮激素应答早期胀泡共延,并且对于发育中的唾液腺中许多随后被激活的晚期基因的胀泡形成和转录是必需的。31个cDNA克隆的定位表明,基因组中约100 kb用于许多BR-C RNA的合成。对这些cDNA克隆的序列分析表明,BR-C编码一族相关蛋白,其特征是一个共同的核心氨基末端结构域与交替的羧基结构域融合,每个羧基结构域包含一对锌指。大多数蛋白质在共同核心区域和锌指区域之间还含有富含独特氨基酸的结构域。由2B5处的染色体重排产生的BR-C突变等位基因与5'-非翻译序列的缺失、核心编码结构域与下游锌指结构域的分离或锌指编码序列的P元件插入破坏有关。我们推断,BR-C通过指定一族具有DNA结合潜能的蛋白质的合成来直接调节晚期基因表达。