Regler R, Sickinger S, Schweizer M
Institut für Mikrobiologie und Biochemie der Universität Erlangen-Nürnberg, Germany.
FEBS Lett. 1991 May 6;282(2):368-72. doi: 10.1016/0014-5793(91)80515-5.
Screening of two rat liver cDNA libraries, one of which was constructed using an alpha 1-inhibitor 3 (alpha 1-13) specific primer, yielded overlapping cDNA clones which correspond to the full length cDNA for alpha 1-13 mRNA. On the basis of sequence microheterogeneity existing throughout the cDNA sequence we identified two alpha 1-13 mRNA species whose sequences are so grossly different in their bait regions that the amino acid homology therein is only 30%. Using oligonucleotide probes derived from their respective bait regions we investigated the regulation of the two alpha 1 I3 mRNA species and demonstrated that only one of them, alpha 1-I3 variant I, is regulated pretranslationally following experimentally induced inflammation.
对两个大鼠肝脏cDNA文库进行筛选,其中一个文库是使用α1-抑制剂3(α1-13)特异性引物构建的,得到了重叠的cDNA克隆,这些克隆对应于α1-13 mRNA的全长cDNA。基于整个cDNA序列中存在的序列微异质性,我们鉴定出两种α1-13 mRNA种类,它们在诱饵区域的序列差异非常大,以至于其中的氨基酸同源性仅为30%。使用源自它们各自诱饵区域的寡核苷酸探针,我们研究了这两种α1 I3 mRNA种类的调控,并证明在实验性诱导炎症后,其中只有一种,即α1-I3变体I,在翻译前受到调控。