聚合酶
RNA聚合酶
基因
RNA聚合酶Ⅱ
遗传学
核小体
RNA聚合酶Ⅲ
生物
计算生物学
核糖核酸
染色质
基因表达
发起人
作者
B.J. Chen,Raghuvar Dronamraju,Whitney R. Smith-Kinnaman,Sarah A. Peck Justice,Austin J. Hepperla,Heather K. MacAlpine,Jeremy M. Simon,Amber L. Mosley,David M. MacAlpine,Brian D. Strahl
标识
DOI:10.1016/j.jbc.2025.108436
摘要
Spt6-Spn1 is an essential histone chaperone complex that associates with RNA Polymerase II (RNAPII) and reassembles nucleosomes during gene transcription. While the interaction between Spt6 and Spn1 is important for its histone deposition and transcription functions, a precise mechanistic understanding is still limited. Here, using temperature sensitive alleles of spt6 and spn1 that disrupt their interaction in yeast, we show that Spt6-Spn1 association is important for its stable interaction with the elongating RNAPII complex and nucleosomes. Using micrococcal nuclease (MNase)-based chromatin occupancy profiling, we further find that Spt6-Spn1 interaction is required to maintain a preferred nucleosome positioning at actively transcribed genes; in the absence of Spt6-Spn1 interaction, we observe a return to replication-dependent phasing. In addition to positioning defects, Spt6-Spn1 disrupting mutants also resulted in an overall shift of nucleosomes towards the 5' end of genes that was correlated with decreased RNAPII levels. As loss of Spt6-Spn1 association results in cryptic transcription at a subset of genes, we examined these genes for their nucleosome profiles. These findings revealed that the chromatin organization at these loci is similar to other active genes, thus underscoring the critical role of DNA sequence in mediating cryptic transcription when nucleosome positioning is altered. Taken together, these findings reveal Spt6-Spn1 interaction is key to its association with elongating RNAPII and for its ability to precisely organize nucleosomes across transcription units.
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