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A core complex of CPSF73 CPSF100 and Symplekin may form two different cleavage factors for processing of poly(A) and histone mRNAs

机译:复杂CpsF73CpsF100和symplekin的芯可以形成两个不同切割因子多聚(a)和组蛋白的mRNa的加工

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摘要

Metazoan histone mRNAs are unique: their pre-mRNAs contain no introns and the mRNAs are not polyadenylated ending instead in a conserved stem-loop structure. In Drosophila, canonical poly(A) signals are located downstream of the normal cleavage site of each histone gene, and are utilized when histone 3’end formation is inhibited. Here we define a sub-complex of poly(A) factors required for histone pre-mRNA processing. We demonstrate that Symplekin, CPSF73 and CPSF100 are present in a stable complex and interact with histone specific processing factors. We use chromatin immunoprecipitation to show that Symplekin and CPSF73, but not CstF50, cotranscriptionally associate with histone genes. Depletion of SLBP recruits CstF50 to histone genes. Knockdown of CPSF160 or CstF64 downregulates Symplekin but does not affect histone pre-mRNA processing or association of Symplekin with the histone locus. These results suggest that a common core cleavage factor is required for processing of histone and polyadenylated pre-mRNAs.

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