The RNA helicase DDX39 contributes to the nuclear export of spliceosomal U snRNA by loading of PHAX onto RNA

Author:

Taniguchi Ichiro12ORCID,Hirose Tetsuro23ORCID,Ohno Mutsuhito1

Affiliation:

1. Institute for Life and Medical Sciences, Kyoto University , Kyoto 606-8507 , Japan

2. Graduate School of Frontier Biosciences, Osaka University , Suita 565-0871 , Japan

3. Institute for Open and Transdisciplinary Research Initiatives, Osaka University , Suita 565-0871 , Japan

Abstract

Abstract RNA helicases are involved in RNA metabolism in an ATP-dependent manner. Although many RNA helicases unwind the RNA structure and/or remove proteins from the RNA, some can load their interacting proteins onto RNAs. Here, we developed an in vitro strategy to identify the ATP-dependent factors involved in spliceosomal uridine-rich small nuclear RNA (U snRNA) export. We identified the RNA helicase UAP56/DDX39B, a component of the mRNA export complex named the transcription-export (TREX) complex, and its closely related RNA helicase URH49/DDX39A as the factors that stimulated RNA binding of PHAX, an adapter protein for U snRNA export. ALYREF, another TREX component, acted as a bridge between PHAX and UAP56/DDX39B. We also showed that UAP56/DDX39B and ALYREF participate in U snRNA export through a mechanism distinct from that of mRNA export. This study describes a novel aspect of the TREX components for U snRNP biogenesis and highlights the loading activity of RNA helicases.

Funder

JSPS

KAKENHI

MEXT

CREST

AMED

Japan Foundation for Applied Enzymology

Narishige Zoological Science Award

Publisher

Oxford University Press (OUP)

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