SAF-B protein couples transcription and pre-mRNA splicing to SAR/MAR elements

被引:154
作者
Nayler, O
Strätling, W
Bourquin, JP
Stagljar, I
Lindemann, L
Jasper, H
Hartmann, AM
Fackelmayer, FO
Ullrich, A
Stamm, S
机构
[1] Max Planck Inst Neurobiol, D-82152 Martinsried, Germany
[2] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[3] Univ Konstanz, Dept Biol, D-78457 Constance, Germany
[4] Univ Zurich, Inst Mol Biol, Dept 2, CH-8057 Zurich, Switzerland
[5] Inst Physiol Chem, D-20246 Hamburg, Germany
关键词
D O I
10.1093/nar/26.15.3542
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
Interphase chromatin is arranged into topologically separated domains comprising gene expression and replication units through genomic sequence elements, so-called MAR or SAR regions (for matrix- or scaffold-associating regions). S/MAR regions are located near the boundaries of actively transcribed genes and were shown to influence their activity. We show that scaffold attachment factor B (SAF-B), which specifically binds to S/MAR regions, interacts with RNA polymerase II (RNA pol II) and a subset of serine-/arginine-rich RNA processing factors (SR proteins). SAF-B localized to the nucleus in a speckled pattern that coincided with the distribution of the SR protein SC35. Furthermore, we show that overexpressed SAF-B induced an increase of the 10S splice product using an E1A reporter gene and repressed the activity of an S/MAR flanked CAT reporter gene construct in vivo. This indicates an association of SAF-B with SR proteins and components of the transcription machinery. Our results describe the coupling of a chromatin organizing S/MAR element with transcription and pre-mRNA processing components and we propose that SAFE serves as a molecular base to assemble a 'transcriptosome complex' in the vicinity of actively transcribed genes.
引用
收藏
页码:3542 / 3549
页数:8
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