首页> 美国卫生研究院文献>Nucleic Acids Research >Cloning of cDNAs coding for human HMG I and HMG Y proteins: both are capable of binding to the octamer sequence motif.
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Cloning of cDNAs coding for human HMG I and HMG Y proteins: both are capable of binding to the octamer sequence motif.

机译:克隆编码人类HMG I和HMG Y蛋白的cDNA:两者均能够结合八聚体序列基序。

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摘要

In human B lymphocytes and placenta HMG I and its smaller isoform HMG Y are encoded by two distinct but structurally highly similar mRNAs which arise most likely by alternative splicing of a single primary transcript. Both have been cloned as cDNAs. On Northern blots an abundant mRNA species 2000 nucleotides in length was detected in all cell lines examined. Exclusively in erythroid cells an additional rare 3800 nucleotides long mRNA species was noted. In quiescent cells the mRNA levels of HMG I/Y were not significantly down-regulated. Southern blot analysis indicated that at least four genes are present per haploid human genome. Both proteins when expressed in bacteria bind specifically to A-T rich stretches of DNA suggesting that no posttranslational modifications are necessary for specific DNA binding. Interestingly, HMG I as well as HMG Y are capable of binding to the octamer transcriptional regulatory sequence motif.
机译:在人B淋巴细胞和胎盘中,HMG I及其较小的亚型HMG Y由两个截然不同但结构高度相似的mRNA编码,这很可能是由单个初级转录本的可变剪接引起的。两者均已被克隆为cDNA。在Northern印迹上,在所有检查的细胞系中检测到了丰富的mRNA种类,长度为2000个核苷酸。仅在红系细胞中发现了另外一个罕见的3800个核苷酸长的mRNA物种。在静止细胞中,HMG I / Y的mRNA水平没有明显下调。 Southern印迹分析表明每个单倍体人类基因组至少存在四个基因。当在细菌中表达时,两种蛋白都与富含A-T的DNA片段特异性结合,这表明翻译后修饰对于特异性DNA结合而言不是必需的。有趣的是,HMG I和HMG Y都能够结合八聚体转录调节序列基序。

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