Koch Henrik, Raabe Monika, Urlaub Henning, Bindereif Albrecht, Preußer Christian
a Institute of Biochemistry, Justus Liebig University of Giessen , D-35392 Giessen , Germany.
b Bioanalytical Mass Spectrometry Group, Max Planck Institute for Biophysical Chemistry , D-37077 Göttingen , Germany.
RNA Biol. 2016;13(2):221-31. doi: 10.1080/15476286.2015.1130208.
The generation of mature mRNA in the protozoan parasite Trypanosoma brucei requires coupled polyadenylation and trans splicing. In contrast to other eukaryotes, we still know very little on components, mechanisms, and dynamics of the 3' end-processing machinery in trypanosomes. To characterize the catalytic core of the polyadenylation complex in T. brucei, we first identified the poly(A) polymerase [Tb927.7.3780] as the major functional, nuclear-localized enzyme in trypanosomes. In contrast, another poly(A) polymerase, encoded by an intron-containing gene [Tb927.3.3160], localizes mainly in the cytoplasm and appears not to be functional in general 3' end processing of mRNAs. Based on tandem-affinity purification with tagged CPSF160 and mass spectrometry, we identified ten associated components of the trypanosome polyadenylation complex, including homologues to all four CPSF subunits, Fip1, CstF50/64, and Symplekin, as well as two hypothetical proteins. RNAi-mediated knockdown revealed that most of these factors are essential for growth and required for both in vivo polyadenylation and trans splicing, arguing for a general coupling of these two mRNA-processing reactions.
原生动物寄生虫布氏锥虫中成熟mRNA的产生需要多腺苷酸化和反式剪接偶联。与其他真核生物不同,我们对锥虫3'端加工机制的组成成分、机制和动力学仍然知之甚少。为了表征布氏锥虫多腺苷酸化复合物的催化核心,我们首先确定了多聚腺苷酸聚合酶[Tb927.7.3780]是锥虫中主要的功能性核定位酶。相比之下,另一种由含内含子基因[Tb927.3.3160]编码的多聚腺苷酸聚合酶主要定位于细胞质,并且在mRNA的一般3'端加工中似乎没有功能。基于用标记的CPSF160进行的串联亲和纯化和质谱分析,我们鉴定了锥虫多腺苷酸化复合物的十个相关成分,包括所有四个CPSF亚基、Fip1、CstF50/64和Symplekin的同源物,以及两种假定蛋白。RNA干扰介导的敲低表明,这些因子中的大多数对生长至关重要,并且是体内多腺苷酸化和反式剪接所必需的,这表明这两种mRNA加工反应普遍偶联。