Mitsialis S A, Spoerel N, Leviten M, Kafatos F C
Department of Cellular and Developmental Biology, Harvard University, Cambridge, MA 02138.
Proc Natl Acad Sci U S A. 1987 Nov;84(22):7987-91. doi: 10.1073/pnas.84.22.7987.
Fusions with the bacterial gene for chloramphenicol acetyltransferase followed by P-element-mediated germ-line transformation in Drosophila have permitted localization of the DNA sequence that confers a high degree of developmental specificity on a pair of silkmoth eggshell (chorion) genes. The short, 272-base-pair, 5'-flanking region shared by the divergently transcribed genes is sufficient for developmentally appropriate expression when placed upstream of the chloramphenicol acetyltransferase gene, in either orientation. A highly conserved motif within that region, TCACGT, is essential for chorion-specific expression.
将氯霉素乙酰转移酶的细菌基因进行融合,随后通过P因子介导在果蝇中进行种系转化,从而定位了一段DNA序列,该序列赋予了一对家蚕卵壳(绒毛膜)基因高度的发育特异性。这两个反向转录基因共有的短的272个碱基对的5'侧翼区域,当置于氯霉素乙酰转移酶基因上游时,无论方向如何,都足以实现发育过程中的适当表达。该区域内一个高度保守的基序TCACGT对于绒毛膜特异性表达至关重要。