Séraphin B, Rosbash M
Department of Biology, Brandeis University, Waltham, MA 02254.
Gene. 1989 Oct 15;82(1):145-51. doi: 10.1016/0378-1119(89)90039-5.
In recent experiments we have used the power of yeast genetics to study U1 small nuclear RNA (snRNA): pre-messenger RNA (pre-mRNA) base pairing interactions [Séraphin et al. EMBO J. 7 (1988) 2533-2538]. Here we extend these observations to other potential U1 snRNA: pre-mRNA pairings. We show that several U1 snRNA mutants are viable. Using these U1 mutant strains we demonstrate further a base-pairing interaction between U1 snRNA position 3 and intron position 6. However, this interaction is only detected with a poor splicing substrate containing branchpoint mutations. These results provide information on the mechanism of 5' splice site-branch point interaction. We also propose several models which may explain why the sequence of the 5' end of the U1 snRNA is conserved among organisms as divergent as man and yeast.
在最近的实验中,我们利用酵母遗传学的力量来研究U1小核RNA(snRNA):前体信使RNA(pre-mRNA)的碱基配对相互作用[Séraphin等人,《欧洲分子生物学组织杂志》7(1988年)2533 - 2538]。在此,我们将这些观察结果扩展到其他潜在的U1 snRNA:pre-mRNA配对。我们发现几个U1 snRNA突变体是有活力的。利用这些U1突变菌株,我们进一步证明了U1 snRNA第3位与内含子第6位之间的碱基配对相互作用。然而,这种相互作用仅在含有分支点突变的较差剪接底物中被检测到。这些结果提供了有关5'剪接位点 - 分支点相互作用机制的信息。我们还提出了几个模型,这些模型可能解释了为什么U1 snRNA 5'端的序列在像人类和酵母这样差异很大的生物体中是保守的。