Hovemann B, Galler R
Nucleic Acids Res. 1982 Apr 10;10(7):2261-74. doi: 10.1093/nar/10.7.2261.
Clones of genes coding for two of the yolk protein precursors from Drosophila melanogaster, YPI and YPII have been isolated. A single small intron was located in the YPII coding region at about the same position as it is found in YPI (6). The entire intergenic spacer region and most of the exon I from the YPII gene have been sequenced. The "capping" sites for both mRNAs have been determined using the S1 protection and cDNA synthesis methods. Comparison of the sequences which might be involved in transcriptional or translational control of these genes reveals for YPII a Hogness Goldberg box but no indication for a conserved sequence around-70-80 (CAT box). In contrast to YPI it resembles no significant homology to the 3' end of 18S rRNA. The first 60 amino acids of exon I from both genes share little homology except for the hydrophobic amino acids which should be involved in protein secretion.
已分离出编码黑腹果蝇两种卵黄蛋白前体YPI和YPII的基因克隆。在YPII编码区发现一个小内含子,其位置与YPI中的大致相同(6)。已对整个基因间隔区和YPII基因的大部分外显子I进行了测序。使用S1保护和cDNA合成方法确定了两种mRNA的“加帽”位点。对可能参与这些基因转录或翻译控制的序列进行比较,发现YPII有一个霍格内斯-戈德堡盒,但未发现-70 - 80周围有保守序列(CAT盒)。与YPI不同,它与18S rRNA的3'端没有明显同源性。两个基因外显子I的前60个氨基酸除了参与蛋白质分泌的疏水氨基酸外,几乎没有同源性。