Department of Genetics, Downing Street, Cambridge CB2 3EH, UK.
EMBO J. 1987 May;6(5):1393-401. doi: 10.1002/j.1460-2075.1987.tb02380.x.
Clones homologous to the 5' region of the Ultrabithorax gene of Drosophila melanogaster have been isolated from D. pseudoobscura, D. funebris and Musca domestica. Regions that encode most of the Ubx protein have been sequenced in all three of these species, and the 5' upstream region has been sequenced in D. funebris to a point 1000 bases upstream of the probable mRNA start site. Here we compare these sequences with those described elsewhere for D. melanogaster. Deduced amino acid sequences of the Ubx protein show 8% (D. pseudoobscura), 15% (D. funebris) and 22% (M. domestica) divergence from D. melanogaster. However, these figures mask very different rates of evolution in different regions of the protein. A glycine-rich (;hinge') region is conserved in each of these species, although its length is variable. Comparison of D. funebris and D. melanogaster sequences in the long 5' untranslated leader region of the mRNA, and in the region immediately upstream of the start point of transcription, reveals tightly conserved elements embedded in an otherwise non-homologous sequence. These conserved elements include a 118-bp region that spans the mRNA start site, an internally repetitive (TAA)(n) region in the untranslated leader and a short repeated motif immediately upstream of the ATG codon that initiates the major open reading frame of the Ubx protein. Two other conserved elements were identified upstream of the transcription start site; both elements have structural features consistent with a role as recognition sites for regulatory proteins.
已从黑腹果蝇的 Ultrabithorax 基因 5' 区同源克隆中分离出与黑腹果蝇、暗褐蜚蠊和家蝇的克隆。在这三个物种中,已对编码 Ubx 蛋白大部分序列的区域进行了测序,并且在暗褐蜚蠊中已对可能的 mRNA 起始位点上游 1000 个碱基的 5' 上游区域进行了测序。在这里,我们将这些序列与其他地方描述的黑腹果蝇的序列进行了比较。推断出的 Ubx 蛋白的氨基酸序列显示,与黑腹果蝇相比,暗褐蜚蠊、黑腹果蝇和家蝇分别有 8%、15%和 22%的差异。然而,这些数字掩盖了蛋白质不同区域的非常不同的进化速度。在这些物种中,一个富含甘氨酸的(hinge)区域在每个物种中都保守,尽管其长度是可变的。在 mRNA 的长 5' 非翻译前导区和转录起始点上游的区域中,比较黑腹果蝇和暗褐蜚蠊的序列,揭示了在其他非同源序列中嵌入的紧密保守元件。这些保守元件包括跨越 mRNA 起始位点的 118 个碱基对区域、非翻译前导区中内部重复的(TAA)(n)区域以及在起始 Ubx 蛋白主要开放阅读框的 ATG 密码子上游的短重复基序。在转录起始点上游还鉴定出另外两个保守元件;这两个元件都具有与作为调节蛋白识别位点的结构特征。