Cargando…

Gene-specific RNA pol II phosphorylation and the "CTD code"

Dynamic phosphorylation of the RNA polymerase II CTD repeats (YS(2)PTS(5)PS(7)) is coupled to transcription and may act as a “code” that controls mRNA synthesis and processing. To examine the "code" in budding yeast, we mapped genome-wide CTD S2, 5 and 7 phosphorylations (PO4) and compared...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Hyunmin, Erickson, Benjamin, Luo, Weifei, Seward, David, Graber, Joel H., Pollock, David, Megee, Paul C., Bentley, David L.
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048030/
https://www.ncbi.nlm.nih.gov/pubmed/20835241
http://dx.doi.org/10.1038/nsmb.1913
Descripción
Sumario:Dynamic phosphorylation of the RNA polymerase II CTD repeats (YS(2)PTS(5)PS(7)) is coupled to transcription and may act as a “code” that controls mRNA synthesis and processing. To examine the "code" in budding yeast, we mapped genome-wide CTD S2, 5 and 7 phosphorylations (PO4) and compared them with the CTD-associated termination factors, Nrd1 and Pcf11. CTD-PO4 dynamics are not scaled to the size of the gene. At 5’ ends, the onset of S2-PO4 is delayed by about 450 bases relative to S5-PO4, regardless of gene length. Phospho-CTD dynamics are gene-specific, with high S5/7-PO4 at the 5' end being characteristic of well-expressed genes with nucleosome-occupied promoters. Furthermore, the CTD kinases Kin28 and Ctk1 profoundly affect pol II distribution along genes in a highly gene-specific way. The "code" is therefore written differently on different genes, probably under the control of promoters. S7-PO4 is enriched on introns and at sites of Nrd1 accumulation suggesting that this modification may function in splicing and Nrd1 recruitment. Nrd1 and Pcf11 frequently co-localized, suggesting functional overlap between these terminators. Surprisingly, Pcf11 is also recruited to centromeres and pol III transcribed genes.