Swi/Snf chromatin remodeling regulates transcriptional interference and gene repression

被引:1
|
作者
Morse, Kaitlin [1 ]
Bishop, Alena L. [1 ]
Swerdlow, Sarah [1 ]
Leslie, Jessica M. [1 ]
Unal, Elcin [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Barker Hall, Berkeley, CA 94720 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
RNA-POLYMERASE-II; SACCHAROMYCES-CEREVISIAE; MESSENGER-RNA; COMPLEX; PROTEIN; YEAST; TRANSLATION; ELONGATION; STRESS; VISUALIZATION;
D O I
10.1016/j.molcel.2024.06.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alternative transcription start sites can affect transcript isoform diversity and translation levels. In a recently described form of gene regulation, coordinated transcriptional and translational interference results in transcript isoform-dependent changes in protein expression. Specifically, a long undecoded transcript isoform (LUTI) is transcribed from a gene-distal promoter, interfering with expression of the gene-proximal promoter. Although transcriptional and chromatin features associated with LUTI expression have been described, the mechanism underlying LUTI-based transcriptional interference is not well understood. Using an unbiased genetic approach followed by functional genomics, we uncovered that the Swi/Snf chromatin remodeling complex is required for co-transcriptional nucleosome remodeling that leads to LUTI-based repression. We identified genes with tandem promoters that rely on Swi/Snf function for transcriptional interference during protein folding stress, including LUTI-regulated genes. This study provides clear evidence for Swi/Snf playing a direct role in gene repression via a cis transcriptional interference mechanism.
引用
收藏
页数:28
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