Saumweber H, Frasch M, Korge G
Institut für Entwicklungsphysiologie Universität zu Köln, Federal Republic of Germany.
Chromosoma. 1990 Apr;99(1):52-60. doi: 10.1007/BF01737289.
The Drosophila nuclear proteins Bj6 and Bx42 characterized previously are detected in a series of developmentally active puffs on salivary gland chromosomes. Here the binding of both proteins at puff 3C11-12 containing the glue protein gene Sgs-4 is described in more detail. By deletion analysis we show that both proteins bind within a chromosomal segment containing 17-19 kb of DNA surrounding the Sgs-4 gene. They are detectable at this site during the intermoult stages, before the puff regresses in response to the moulting hormone ecdysone. If the Sgs-4 gene together with flanking DNA sequences is brought into a different chromosomal position by P element transfer, both proteins are detected at this new location. Both proteins are bound to the chromosome within the range of 2.5 kb DNA upstream of the Sgs-4 gene. A strain containing a 52 bp deletion within this region fails to bind Bx42 protein suggesting that the missing DNA, which overlaps a hypersensitive region, may be required for the binding of the Bx42 protein.
先前鉴定的果蝇核蛋白Bj6和Bx42在唾液腺染色体上一系列发育活跃的胀泡中被检测到。本文更详细地描述了这两种蛋白在含有胶蛋白基因Sgs-4的3C11-12胀泡处的结合情况。通过缺失分析,我们发现这两种蛋白都结合在围绕Sgs-4基因的一段17-19 kb的染色体DNA片段内。在蜕皮激素作用下胀泡消退之前的蜕皮间期,可在该位点检测到它们。如果通过P因子转移将Sgs-4基因及其侧翼DNA序列置于不同的染色体位置,在这个新位置也能检测到这两种蛋白。这两种蛋白都结合在Sgs-4基因上游2.5 kb DNA范围内的染色体上。在该区域含有一个52 bp缺失的菌株无法结合Bx42蛋白,这表明与一个超敏区域重叠的缺失DNA可能是Bx42蛋白结合所必需的。