Chu Yaya, Simic Rajna, Warner Marcie H, Arndt Karen M, Prelich Gregory
Department of Molecular Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
EMBO J. 2007 Nov 14;26(22):4646-56. doi: 10.1038/sj.emboj.7601887. Epub 2007 Oct 18.
The Bur1-Bur2 and Paf1 complexes function during transcription elongation and affect histone modifications. Here we describe new roles for Bur1-Bur2 and the Paf1 complex. We find that histone H3 K36 tri-methylation requires specific components of the Paf1 complex and that K36 tri-methylation is more strongly affected at the 5' ends of genes in paf1delta and bur2delta strains in parallel with increased acetylation of histones H3 and H4. Interestingly, the 5' increase in histone acetylation is independent of K36 methylation, and therefore is mechanistically distinct from the methylation-driven deacetylation that occurs at the 3' ends of genes. Finally, Bur1-Bur2 and the Paf1 complex have a second methylation-independent function, since bur2delta set2delta and paf1delta set2delta double mutants display enhanced histone acetylation at the 3' ends of genes and increased cryptic transcription initiation. These findings identify new functions for the Paf1 and Bur1-Bur2 complexes, provide evidence that histone modifications at the 5' and 3' ends of coding regions are regulated by distinct mechanisms, and reveal that the Bur1-Bur2 and Paf1 complexes repress cryptic transcription through a Set2-independent pathway.
Bur1-Bur2复合物和Paf1复合物在转录延伸过程中发挥作用,并影响组蛋白修饰。在此,我们描述了Bur1-Bur2复合物和Paf1复合物的新功能。我们发现组蛋白H3 K36三甲基化需要Paf1复合物的特定组分,并且在paf1δ和bur2δ菌株中,基因5'端的K36三甲基化受到的影响更强,同时组蛋白H3和H4的乙酰化增加。有趣的是,组蛋白乙酰化在5'端的增加与K36甲基化无关,因此在机制上不同于在基因3'端发生的甲基化驱动的去乙酰化。最后,Bur1-Bur2复合物和Paf1复合物具有第二种不依赖于甲基化的功能,因为bur2δ set2δ和paf1δ set2δ双突变体在基因3'端显示出增强的组蛋白乙酰化和增加的隐蔽转录起始。这些发现确定了Paf1复合物和Bur1-Bur2复合物的新功能,提供了证据表明编码区5'端和3'端的组蛋白修饰受不同机制调控,并揭示了Bur1-Bur2复合物和Paf1复合物通过一条不依赖于Set2的途径抑制隐蔽转录。