Hampson R K, La Follette L, Rottman F M
Department of Molecular Biology and Microbiology, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.
Mol Cell Biol. 1989 Apr;9(4):1604-10. doi: 10.1128/mcb.9.4.1604-1610.1989.
In a previous report, we described the presence, in pituitary tissue, of an alternatively processed species of bovine growth hormone mRNA from which the last intron (intron D) has not been removed by splicing (R. K. Hampson and F. M. Rottman, Proc. Natl. Acad. Sci. USA 84:2673-2677, 1987). Using transient expression of the bovine growth hormone gene in Cos I cells, we observed that splicing of intron D was affected by sequences within the downstream exon (exon 5). Deletion of a 115-base-pair FspI-PvuII restriction fragment in exon 5 beginning 73 base pairs downstream of the intron 4-exon 5 junction resulted in cytoplasmic bovine growth hormone mRNA, more than 95% of which retained intron D. This contrasted with less than 5% of the growth hormone mRNA retaining intron D observed with expression of the unaltered gene. Insertion of a 10-base-pair inverted repeat sequence, CTTCCGGAAG, which was located in the middle of this deleted segment, partially reversed this pattern, resulting in cytosolic mRNA from which intron D was predominantly removed. More detailed deletion analysis of this region indicated that multiple sequence elements within the exon 5, in addition to the 10-base-pair inverted repeat sequence, are capable of influencing splicing of intron D. The effect of these exon sequences on splicing of bovine growth hormone precursor mRNA appeared to be specific for the growth hormone intron D. Deletions in exon 5 which resulted in marked alterations in splicing of growth hormone intron D had no effect on splicing when exon 5 of bovine growth hormone was placed downstream of the heterologous bovine prolactin intron D. Deletions in exon 5 which resulted in marked alterations in splicing of growth hormone intron D had no effect on splicing when exon 5 of bovine growth hormone was placed downstream of the heterologous bovine prolactin intron D. The results of this study suggest a unique interaction between sequences located near the center of exon 5 and splicing of the adjacent intron D.
在之前的一份报告中,我们描述了在垂体组织中存在一种经过可变加工的牛生长激素mRNA,其最后一个内含子(内含子D)未通过剪接去除(R.K.汉普森和F.M.罗特曼,《美国国家科学院院刊》84:2673 - 2677,1987)。通过在Cos I细胞中瞬时表达牛生长激素基因,我们观察到内含子D的剪接受下游外显子(外显子5)内序列的影响。从内含子4 - 外显子5连接处下游73个碱基对开始,删除外显子5中一个115碱基对的FspI - PvuII限制片段,导致细胞质中的牛生长激素mRNA,其中超过95%保留了内含子D。这与未改变基因表达时观察到的不到5%的生长激素mRNA保留内含子D形成对比。在这个缺失片段中间插入一个10碱基对的反向重复序列CTTCCGGAAG,部分逆转了这种模式,导致细胞质mRNA中内含子D主要被去除。对该区域更详细的缺失分析表明,除了10碱基对的反向重复序列外,外显子5内的多个序列元件能够影响内含子D的剪接。这些外显子序列对牛生长激素前体mRNA剪接的影响似乎对生长激素内含子D具有特异性。当牛生长激素的外显子5置于异源牛催乳素内含子D下游时,外显子5中导致生长激素内含子D剪接显著改变的缺失对剪接没有影响。这项研究的结果表明外显子5中心附近的序列与相邻内含子D的剪接之间存在独特的相互作用。