Dominski Zbigniew, Marzluff William F
Program in Molecular Biology and Biotechnology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Gene. 2007 Jul 15;396(2):373-90. doi: 10.1016/j.gene.2007.04.021. Epub 2007 May 4.
Nearly all eukaryotic mRNAs end with a poly(A) tail that is added to their 3' end by the ubiquitous cleavage/polyadenylation machinery. The only known exceptions to this rule are metazoan replication-dependent histone mRNAs, which end with a highly conserved stem-loop structure. This distinct 3' end is generated by specialized 3' end processing machinery that cleaves histone pre-mRNAs 4-5 nucleotides downstream of the stem-loop and consists of the U7 small nuclear RNP (snRNP) and number of protein factors. Recently, the U7 snRNP has been shown to contain a unique Sm core that differs from that of the spliceosomal snRNPs, and an essential heat labile processing factor has been identified as symplekin. In addition, cross-linking studies have pinpointed CPSF-73 as the endonuclease, which catalyzes the cleavage reaction. Thus, many of the critical components of the 3' end processing machinery are now identified. Strikingly, this machinery is not as unique as initially thought but contains at least two factors involved in cleavage/polyadenylation, suggesting that the two mechanisms have a common evolutionary origin. The greatest challenge that lies ahead is to determine how all these factors interact with each other to form a catalytically competent processing complex capable of cleaving histone pre-mRNAs.
几乎所有真核生物的信使核糖核酸(mRNA)都以聚腺苷酸(poly(A))尾巴结尾,该尾巴由普遍存在的切割/聚腺苷酸化机制添加到其3'末端。这条规则唯一已知的例外是后生动物复制依赖型组蛋白mRNA,它们以高度保守的茎环结构结尾。这种独特的3'末端是由专门的3'末端加工机制产生的,该机制在茎环下游4-5个核苷酸处切割组蛋白前体mRNA,由U7小核核糖核蛋白(snRNP)和一些蛋白质因子组成。最近,已证明U7 snRNP含有一个与剪接体snRNP不同的独特Sm核心,并且已确定一种必需的热不稳定加工因子为共生蛋白。此外,交联研究已确定CPSF-73为催化切割反应的核酸内切酶。因此,现在已确定了3'末端加工机制的许多关键成分。引人注目的是,这种机制并不像最初认为的那样独特,而是至少包含两个参与切割/聚腺苷酸化的因子,这表明这两种机制有共同的进化起源。未来最大的挑战是确定所有这些因子如何相互作用,以形成一个能够切割组蛋白前体mRNA的具有催化活性的加工复合体。