Selinger D, Liao X, Wise J A
Department of Biochemistry, University of Illinois, Urbana-Champaign 61801.
Proc Natl Acad Sci U S A. 1993 Jun 15;90(12):5409-13. doi: 10.1073/pnas.90.12.5409.
Signal recognition particle (SRP) RNA exhibits significant primary sequence conservation only in domain IV, a bulged hairpin capped by a GNRA (N, any nucleotide; R, purine) tetranucleotide loop except in plant homologs. Tetraloops conforming to this sequence or to the consensus UNCG enhance the stability of synthetic RNA hairpins and have strikingly similar three-dimensional structures. To determine the biological relevance of this similarity, as well as to assess the relative contributions of sequence and structure to the function of the domain IV tetraloop, we replaced the GAAA sequence in fission yeast SRP RNA with UUCG. Haploid strains harboring this substitution are viable, providing experimental evidence for the functional equivalence of the two tetraloops. We next tested the two sequences found in plant SRP RNAs at this location for function in the context of the Schizosaccharomyces pombe RNA. While substitution of CUUC does not allow growth, a viable strain results from replacing GAAA with UUUC. Although the viable tetraloop substitution mutants exhibit wild-type growth under normal conditions, all three express conditional defects. To determine whether this might be a consequence of structural perturbations, we performed enzymatic probing. The results indicate that RNAs containing tetraloop substitutions exhibit subtle differences from the wild type not only in the tetraloop itself, but also in the 3-base pair adjoining stem. To directly assess the importance of the latter structure, we disrupted it partially or completely and made the compensatory mutations to restore the helix. Surprisingly, mutant RNAs with as little as one Watson-Crick base pair can support growth.
信号识别颗粒(SRP)RNA仅在结构域IV中表现出显著的一级序列保守性,结构域IV是一个由GNRA(N为任意核苷酸;R为嘌呤)四环帽盖的凸起发夹结构,但植物同源物除外。符合该序列或一致序列UNCG的四环增强了合成RNA发夹的稳定性,并且具有惊人相似的三维结构。为了确定这种相似性的生物学相关性,以及评估序列和结构对结构域IV四环功能的相对贡献,我们将裂殖酵母SRP RNA中的GAAA序列替换为UUCG。携带这种替换的单倍体菌株是可行的,为这两个四环的功能等效性提供了实验证据。接下来,我们在粟酒裂殖酵母RNA的背景下测试了植物SRP RNA在该位置发现的两个序列的功能。虽然用CUUC替换不允许生长,但用UUUC替换GAAA会产生一个可行的菌株。尽管可行的四环替换突变体在正常条件下表现出野生型生长,但所有三种突变体都表现出条件性缺陷。为了确定这是否可能是结构扰动的结果,我们进行了酶促探测。结果表明,含有四环替换的RNA不仅在四环本身,而且在相邻茎的3个碱基对中与野生型存在细微差异。为了直接评估后一种结构的重要性,我们部分或完全破坏它,并进行补偿性突变以恢复螺旋结构。令人惊讶的是,只有一个沃森-克里克碱基对的突变RNA就能支持生长。