| Literature DB >> 19217410 |
Yongsheng Shi1, Dafne Campigli Di Giammartino, Derek Taylor, Ali Sarkeshik, William J Rice, John R Yates, Joachim Frank, James L Manley.
Abstract
Pre-mRNA 3' end formation is an essential step in eukaryotic gene expression. Over half of human genes produce alternatively polyadenylated mRNAs, suggesting that regulated polyadenylation is an important mechanism for posttranscriptional gene control. Although a number of mammalian mRNA 3' processing factors have been identified, the full protein composition of the 3' processing machinery has not been determined, and its structure is unknown. Here we report the purification and subsequent proteomic and structural characterization of human mRNA 3' processing complexes. Remarkably, the purified 3' processing complex contains approximately 85 proteins, including known and new core 3' processing factors and over 50 proteins that may mediate crosstalk with other processes. Electron microscopic analyses show that the core 3' processing complex has a distinct "kidney" shape and is approximately 250 A in length. Together, our data has revealed the complexity and molecular architecture of the pre-mRNA 3' processing complex.Entities:
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Year: 2009 PMID: 19217410 PMCID: PMC2946185 DOI: 10.1016/j.molcel.2008.12.028
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970