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编码人类寄生虫曼氏血吸虫卵壳(绒毛膜)蛋白的小基因家族。

Small gene family encoding an eggshell (chorion) protein of the human parasite Schistosoma mansoni.

作者信息

Bobek L A, Rekosh D M, LoVerde P T

机构信息

Department of Microbiology, State University of New York at Buffalo 14214.

出版信息

Mol Cell Biol. 1988 Aug;8(8):3008-16. doi: 10.1128/mcb.8.8.3008-3016.1988.

Abstract

We have isolated six independent genomic clones encoding schistosome chorion or eggshell proteins from a Schistosoma mansoni genomic library. A linkage may of five of the clones spanning 35 kilobase pair (kbp) of the S. mansoni genome was constructed. The region contained two eggshell protein genes closely linked, separated by 7.5 kbp of intergenic DNA. The two genes of the cluster were arranged in the same orientation, that is, they were transcribed from the same strand. The sixth clone probably represents a third copy of the eggshell gene that is not contained within the 35-kbp region. The 5' end of the mRNA transcribed from these genes was defined by primer extension directly off the RNA. The ATCAT cap site sequence was homologous to a silkmoth chorion PuTCATT cap site sequence, where Pu indicates any purine. DNA sequence analysis showed that there were no introns in these genes. The DNA sequences of the three genes were very homologous to each other and to a cDNA clone, pSMf61-46, differing only in three or four nucleotides. A multiple TATA box was located at positions -23 to -31, and a CAAAT sequence was located at -52 upstream of the eggshell transcription unit. Comparison of sequences in regions further upstream with silkmoth and Drosophila sequences revealed several very short elements that were shared. One such element, TCACGT, recently shown to be an essential cis-regulatory element for silkmoth chorion gene promoter function, was found at a similar position in all three organisms.

摘要

我们从曼氏血吸虫基因组文库中分离出了六个独立的基因组克隆,这些克隆编码血吸虫绒毛膜或卵壳蛋白。构建了一个包含五个克隆的连锁图谱,其跨度为曼氏血吸虫基因组的35千碱基对(kbp)。该区域包含两个紧密连锁的卵壳蛋白基因,它们被7.5 kbp的基因间DNA隔开。该基因簇的两个基因以相同的方向排列,也就是说,它们从同一条链转录。第六个克隆可能代表卵壳基因的第三个拷贝,它不在35 kbp区域内。从这些基因转录的mRNA的5'端通过直接从RNA上进行引物延伸来确定。ATCAT帽位点序列与家蚕绒毛膜PuTCATT帽位点序列同源,其中Pu表示任何嘌呤。DNA序列分析表明这些基因中没有内含子。这三个基因的DNA序列彼此之间以及与一个cDNA克隆pSMf61 - 46非常同源,仅在三四个核苷酸上有所不同。一个多个TATA框位于-23至-31位,一个CAAAT序列位于卵壳转录单元上游-52位。将更上游区域的序列与家蚕和果蝇的序列进行比较,发现了几个共享的非常短的元件。其中一个元件TCACGT,最近被证明是家蚕绒毛膜基因启动子功能的一个必需顺式调节元件,在所有三种生物的相似位置都被发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ff/363526/48ec3495ca4b/molcellb00068-0033-a.jpg

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