Kolev Nikolay G, Steitz Joan A
Howard Hughes Medical Institute, Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06536, USA.
Genes Dev. 2005 Nov 1;19(21):2583-92. doi: 10.1101/gad.1371105. Epub 2005 Oct 17.
Most metazoan messenger RNAs encoding histones are cleaved, but not polyadenylated at their 3' ends. Processing in mammalian cell extracts requires the U7 small nuclear ribonucleoprotein (U7 snRNP) and an unidentified heat-labile factor (HLF). We describe the identification of a heat-sensitive protein complex whose integrity is required for histone pre-mRNA cleavage. It includes all five subunits of the cleavage and polyadenylation specificity factor (CPSF), two subunits of the cleavage stimulation factor (CstF), and symplekin. Reconstitution experiments reveal that symplekin, previously shown to be necessary for cytoplasmic poly(A) tail elongation and translational activation of mRNAs during Xenopus oocyte maturation, is the essential heat-labile component. Thus, a common molecular machinery contributes to the nuclear maturation of mRNAs both lacking and possessing poly(A), as well as to cytoplasmic poly(A) tail elongation.
大多数编码组蛋白的后生动物信使核糖核酸(mRNA)在其3'端被切割,但不进行多聚腺苷酸化。在哺乳动物细胞提取物中的加工过程需要U7小核核糖核蛋白(U7 snRNP)和一种未鉴定的热不稳定因子(HLF)。我们描述了一种热敏感蛋白复合物的鉴定,其完整性是组蛋白前体mRNA切割所必需的。它包括切割和多聚腺苷酸化特异性因子(CPSF)的所有五个亚基、切割刺激因子(CstF)的两个亚基和共生蛋白。重组实验表明,共生蛋白是必不可少的热不稳定成分,此前已证明它在非洲爪蟾卵母细胞成熟过程中对mRNA的细胞质多聚(A)尾延长和翻译激活是必需的。因此,一种共同的分子机制有助于缺乏和具有多聚(A)的mRNA的核成熟,以及细胞质多聚(A)尾的延长。