TY - JOUR
T1 - ALYREF mainly binds to the 5′ and the 3′ regions of the mRNA in vivo
AU - Shi, Min
AU - Zhang, Heng
AU - Wu, Xudong
AU - He, Zhisong
AU - Wang, Lantian
AU - Yin, Shanye
AU - Tian, Bin
AU - Li, Guohui
AU - Cheng, Hong
N1 - Funding Information:
This work was supported by grants from National key R&D Program of China [2017YFA0504400]; Ministry of Science and Technology of China [2013CB910402]; National Natural Science Foundation of China [21625302, 31570822, 91540104, 31400676]. Funding for open access charge: National Natural Science Foundation of China [21625302]. Conflict of interest statement. None declared.
Publisher Copyright:
© The Author(s) 2017.
PY - 2017/9/19
Y1 - 2017/9/19
N2 - The TREX complex (TREX) plays key roles in nuclear export of mRNAs. However, little is known about its transcriptome-wide binding targets. We used individual cross-linking and immunoprecipitation (iCLIP) to identify the binding sites of ALYREF, an mRNA export adaptor in TREX, in human cells. Consistent with previous in vitro studies, ALYREF binds to a region near the 5′ end of the mRNA in a CBP80-dependent manner. Unexpectedly, we identified PABPN1-dependent ALYREF binding near the 3′ end of the mRNA. Furthermore, the 3′ processing factor CstF64 directly interacts with ALYREF and is required for the overall binding of ALYREF on the mRNA. In addition, we found that numerous middle exons harbor ALYREF binding sites and identified ALYREF-binding motifs that promote nuclear export of intronless mRNAs. Together, our study defines enrichment of ALYREF binding sites at the 5′ and the 3′ regions of the mRNA in vivo, identifies export-promoting ALYREF-binding motifs, and reveals CstF64- and PABPN1-mediated coupling of mRNA nuclear export to 3′ processing.
AB - The TREX complex (TREX) plays key roles in nuclear export of mRNAs. However, little is known about its transcriptome-wide binding targets. We used individual cross-linking and immunoprecipitation (iCLIP) to identify the binding sites of ALYREF, an mRNA export adaptor in TREX, in human cells. Consistent with previous in vitro studies, ALYREF binds to a region near the 5′ end of the mRNA in a CBP80-dependent manner. Unexpectedly, we identified PABPN1-dependent ALYREF binding near the 3′ end of the mRNA. Furthermore, the 3′ processing factor CstF64 directly interacts with ALYREF and is required for the overall binding of ALYREF on the mRNA. In addition, we found that numerous middle exons harbor ALYREF binding sites and identified ALYREF-binding motifs that promote nuclear export of intronless mRNAs. Together, our study defines enrichment of ALYREF binding sites at the 5′ and the 3′ regions of the mRNA in vivo, identifies export-promoting ALYREF-binding motifs, and reveals CstF64- and PABPN1-mediated coupling of mRNA nuclear export to 3′ processing.
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U2 - 10.1093/nar/gkx597
DO - 10.1093/nar/gkx597
M3 - Article
C2 - 28934468
AN - SCOPUS:85031916796
SN - 0305-1048
VL - 45
SP - 9640
EP - 9653
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 16
ER -