Spoerel N, Nguyen H T, Kafatos F C
J Mol Biol. 1986 Jul 5;190(1):23-35. doi: 10.1016/0022-2836(86)90072-0.
We report on the detailed structural and developmental characterization of four chorion genes and a truncated pseudogene located within a 9.5 X 10(3) base chromosomal segment. These genes belong to the A and B multigene families and, like previously characterized moth chorion genes, are arranged in tightly linked pairs, which are divergently transcribed (A/B.L11 and A/B.L12). On the basis of their high degree of sequence divergence, the A genes define two distinct subfamilies, while the more homologous B genes represent different copies of the same gene type. The A.L11 and B.L11 introns are much longer, in each case because of a single inserted DNA segment that is missing from A.L12 or B.L12. The 2.1 X 10(3) base insertion in A.L11 is the first retrovirus-like transposable element characterized in Bombyx mori. The very short 5' flanking sequences of A/B.L11 and A/B.L12 (277 and 276 base-pairs) are distinct as shown by hybridization but both recur in additional chorion gene pairs, forming two respective classes that are expressed during distinctly different developmental periods. The divergently transcribed genes of each pair, which border the same 5' flanking sequence, are expressed co-ordinately, during the same developmental period. Detailed comparisons of the 5' flanking regions, and of the corresponding region of the Drosophila s15-1 chorion gene, revealed numerous, very short sequence elements that are shared. One such element, T-C-A-C-G-T, is also associated with all five sequenced Drosophila chorion genes. Some elements are repeated in a dyad symmetrical pattern, i.e. are associated with each of the two genes in a pair, while others, including T-C-A-C-G-T, occur only once per 5' flanking region, and, if functionally important, would presumably act bi-directionally on both genes of the pair.
我们报告了位于一个9.5×10³碱基染色体片段内的四个绒毛膜基因和一个截短的假基因的详细结构和发育特征。这些基因属于A和B多基因家族,并且与先前表征的蛾类绒毛膜基因一样,以紧密连锁的对排列,这些对是反向转录的(A/B.L11和A/B.L12)。基于它们高度的序列差异,A基因定义了两个不同的亚家族,而同源性更高的B基因代表相同基因类型的不同拷贝。A.L11和B.L11内含子长得多,在每种情况下都是因为单个插入的DNA片段在A.L12或B.L12中缺失。A.L11中2.1×10³碱基的插入是在家蚕中表征的第一个逆转录病毒样转座元件。A/B.L11和A/B.L12非常短的5'侧翼序列(277和276个碱基对)通过杂交显示是不同的,但两者在其他绒毛膜基因对中再次出现,形成两个各自的类别,在明显不同的发育时期表达。每对反向转录的基因与相同的5'侧翼序列相邻,在同一发育时期协同表达。对5'侧翼区域以及果蝇s15-1绒毛膜基因相应区域的详细比较揭示了许多共享的非常短的序列元件。其中一个这样的元件T-C-A-C-G-T也与所有五个测序的果蝇绒毛膜基因相关。一些元件以二元对称模式重复,即与一对中的两个基因中的每一个相关,而其他元件,包括T-C-A-C-G-T,在每个5'侧翼区域仅出现一次,如果具有功能重要性,则可能对该对中的两个基因都起双向作用。