DeWille J W, Harendza C J, Jenh C H, Johnson L F
Department of Biochemistry and Molecular Genetics, Ohio State University, Columbus 43210.
J Cell Physiol. 1989 Feb;138(2):358-66. doi: 10.1002/jcp.1041380219.
Thymidylate synthase (TS) mRNA content increases about 20-fold when growth-stimulated mouse cells progress from the G0/G1 phase into the S phase of the cell cycle. Previous studies, using a cell line in which the TS gene is amplified (LU3-7), indicated that transcriptional initiation as well as polyadenylation of the mRNA occur at several locations in unsynchronized cells. In the present study, we have used S1 nuclease protection assays to analyze the possible significance of the multiple transcriptional initiation and polyadenylation sites. We found that the same pattern of 5' and 3' termini were detected with RNA isolated from the overproducing cells as with RNA isolated from the parental mouse 3T6 cell line, demonstrating that the heterogeneous termini are not a consequence of gene amplification. There was no change in the pattern of 5' or 3' termini with either cell line during the progression from G1 phase through S phase in serum-stimulated cells. Therefore, the increase in TS mRNA content is not the result of differential utilization of the various transcriptional initiation or polyadenylation sites. Analyses of poly(A)- deficient cytoplasmic TS RNA showed that the 5' termini were the same as those found in poly(A) + mRNA. However, the 3' termini were extremely heterogeneous in length. Although some of the poly(A)- deficient RNA extended beyond the normal site of polyadenylation, most of it was shorter than full-length TS mRNA.
当生长刺激的小鼠细胞从细胞周期的G0/G1期进入S期时,胸苷酸合成酶(TS)mRNA含量增加约20倍。先前使用TS基因被扩增的细胞系(LU3-7)进行的研究表明,mRNA的转录起始以及多聚腺苷酸化在未同步化的细胞中的几个位置发生。在本研究中,我们使用S1核酸酶保护试验来分析多个转录起始和多聚腺苷酸化位点的可能意义。我们发现,从过量产生细胞中分离的RNA与从小鼠亲本3T6细胞系中分离的RNA检测到相同的5'和3'末端模式,表明异质末端不是基因扩增的结果。在血清刺激的细胞从G1期到S期的进程中,两种细胞系的5'或3'末端模式均未发生变化。因此,TS mRNA含量的增加不是各种转录起始或多聚腺苷酸化位点差异利用的结果。对缺乏多聚腺苷酸的细胞质TS RNA的分析表明,5'末端与在多聚腺苷酸+ mRNA中发现的相同。然而,3'末端在长度上极其异质。尽管一些缺乏多聚腺苷酸的RNA延伸超过了正常的多聚腺苷酸化位点,但大多数都比全长TS mRNA短。