Burch J B
Nucleic Acids Res. 1984 Jan 25;12(2):1117-35. doi: 10.1093/nar/12.2.1117.
We have precisely determined the positions of the first three exons for the major chicken vitellogenin gene (VTG II) by a combination of S1 nuclease protection, primer extension and DNA sequencing experiments. In addition, we have determined the nucleotide sequences of the 5' flanking nuclease hypersensitive sites that we have previously shown are induced during the estrogen mediated activation of the VTG II gene in liver (1). One of these sites is found to be nearly identical to the enhancer core sequence of SV40. A computer assisted analysis of the DNA sequences upstream from the VTG II gene has revealed four short (7 to 9 base pair) sequence elements that are present in similar positions flanking the other major estrogen inducible gene for liver, very low density apolipoprotein II (apoVLDL II). For VTG II, these sequences are located between two of the induced nuclease hypersensitive sites that are liver specific. Sequences homologous to one element, located approximately 100 base pairs upstream from the mRNA cap sites of the VTG II and apoVLDL II genes, are also observed for three estrogen inducible genes that are expressed in the oviduct, although for each of these genes the sequence falls further upstream, between -220 and -200. We suggest that these conserved sequences may be important in mediating the tissue specific responses of these genes to estrogen.
我们通过S1核酸酶保护、引物延伸和DNA测序实验相结合的方法,精确确定了主要鸡卵黄蛋白原基因(VTG II)前三个外显子的位置。此外,我们还确定了5'侧翼核酸酶超敏位点的核苷酸序列,我们之前已经证明这些位点是在雌激素介导的肝脏VTG II基因激活过程中诱导产生的(1)。其中一个位点被发现与SV40的增强子核心序列几乎相同。对VTG II基因上游DNA序列的计算机辅助分析揭示了四个短(7至9个碱基对)序列元件,它们在肝脏中另一个主要的雌激素诱导基因——极低密度载脂蛋白II(apoVLDL II)两侧的相似位置出现。对于VTG II,这些序列位于两个肝脏特异性诱导核酸酶超敏位点之间。在输卵管中表达的三个雌激素诱导基因中也观察到了与一个元件同源的序列,该元件位于VTG II和apoVLDL II基因mRNA帽位点上游约100个碱基对处,尽管对于这些基因中的每一个,该序列位于更上游,在-220至-200之间。我们认为这些保守序列可能在介导这些基因对雌激素的组织特异性反应中起重要作用。