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雌激素调节的鸡卵黄蛋白原II基因启动子区域及5'上游去甲基化位点的结构与序列

Structure and sequence of the promoter area and of a 5' upstream demethylation site of the estrogen-regulated chicken vitellogenin ii gene.

作者信息

Geiser M, Mattaj I W, Wilks A F, Seldran M, Jost J P

出版信息

J Biol Chem. 1983 Jul 25;258(14):9024-30.

PMID:6306010
Abstract

We sequenced 487 base pairs (bp) covering the 5' end of chicken vitellogenin II gene and 840 bp of its 5' end-flanking region. This region includes a MspI/HpaII restriction site which becomes undermethylated in chicken liver upon estrogen treatment. Southern blot analysis of restriction enzyme digests of total DNA confirms that this undermethylation site is the one situated at -611 bp from the cap sequence. This site is flanked at nucleotides -567, -629, and -667 by stretches of DNA very rich in A + T. We used S1 nuclease mapping as well as a primer extension procedure to map the transcription starting point of the vitellogenin II gene. We found a 5'CATAAAA3' box between nucleotides -32 and -26, and between nucleotides -77 and -69 a sequence (5'TTGAGAATT3') homologous to the bacterial RNA polymerase-binding site. A similar sequence (5'TGTTTACATAAA3') is also found between nucleotides -101 and -90. A comparison of the sequence of the primer-extended DNA with the 5' end of vitellogenin II gene revealed the presence of two small exons of 53 and 21 bp between nucleotides +1 and +53, and +169 and +189, respectively, and two small introns of 115 and 100 bp between nucleotides +54 and +168, and +190 and +290, respectively. The first AUG at nucleotide +14 is in front of an open reading frame. We found that 77% of the amino acids coded by the first exon are hydrophobic, a feature compatible with a signal sequence of a secreted protein such as vitellogenin.

摘要

我们对覆盖鸡卵黄生成素II基因5'端的487个碱基对(bp)及其5'端侧翼区域的840 bp进行了测序。该区域包含一个MspI/HpaII限制性酶切位点,在雌激素处理后鸡肝脏中该位点会发生去甲基化。对总DNA限制性酶切片段的Southern印迹分析证实,这个去甲基化位点位于距帽序列-611 bp处。该位点在核苷酸-567、-629和-667处两侧是富含A + T的DNA片段。我们使用S1核酸酶图谱分析以及引物延伸程序来确定卵黄生成素II基因的转录起始点。我们在核苷酸-32和-26之间发现了一个5'CATAAAA3'框,在核苷酸-77和-69之间发现了一个与细菌RNA聚合酶结合位点同源的序列(5'TTGAGAATT3')。在核苷酸-101和-90之间也发现了一个类似的序列(5'TGTTTACATAAA3')。将引物延伸DNA的序列与卵黄生成素II基因的5'端进行比较,发现在核苷酸+1和+53之间以及+169和+189之间分别存在两个53 bp和21 bp的小外显子,在核苷酸+54和+168之间以及+190和+290之间分别存在两个115 bp和100 bp的小内含子。核苷酸+14处的第一个AUG位于一个开放阅读框之前。我们发现第一个外显子编码的77%的氨基酸是疏水的,这一特征与分泌蛋白如卵黄生成素的信号序列相符。

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