Symplekin and multiple other polyadenylation factors participate in 3′-end maturation of histone mRNAs
Open Access
- 17 October 2005
- journal article
- Published by Cold Spring Harbor Laboratory in Genes & Development
- Vol. 19 (21) , 2583-2592
- https://doi.org/10.1101/gad.1371105
Abstract
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.Keywords
This publication has 64 references indexed in Scilit:
- Symplekin and xGLD-2 Are Required for CPEB-Mediated Cytoplasmic PolyadenylationCell, 2004
- HSF1 Modulation of Hsp70 mRNA Polyadenylation via Interaction with SymplekinJournal of Biological Chemistry, 2004
- Symplekin, a Constitutive Protein of Karyo- and Cytoplasmic Particles Involved in mRNA Biogenesis inXenopus laevisOocytesMolecular Biology of the Cell, 2002
- A novel zinc finger protein is associated with U7 snRNP and interacts with the stem–loop binding protein in the histone pre-mRNP to stimulate 3′-end processingGenes & Development, 2002
- Multiple interactions of the transcription factor YY1 with human histone H4 gene regulatory elementsJournal of Cellular Biochemistry, 1999
- Symplekin, a novel type of tight junction plaque protein.The Journal of cell biology, 1996
- Multiple processing-defective mutations in a mammalian histone pre-mRNA are suppressed by compensatory changes in U7 RNA both in vivo and in vitro.Genes & Development, 1991
- Identification of the Human U7 snRNP as One of Several Factors Involved in the 3′ End Maturation of Histone Premessenger RNA'sScience, 1987
- Compensatory mutations suggest that base-pairing with a small nuclear RNA is required to form the 3′ end of H3 messenger RNANature, 1986
- Formation of the 3′ end of histone mRNA by post-transcriptional processingNature, 1984