Probable ATP-dependent RNA helicase DDX17
Also known as: DDX17
Function
As an RNA helicase, unwinds RNA and alters RNA structures through ATP binding and hydrolysis. Involved in multiple cellular processes, including pre-mRNA splicing, alternative splicing, ribosomal RNA processing and miRNA processing, as well as transcription regulation. Regulates the alternative splicing of exons exhibiting specific features. For instance, promotes the inclusion of AC-rich alternative exons in CD44 transcripts. This function requires the RNA helicase activity. Affects NFAT5 and histone macro-H2A.1/MACROH2A1 alternative splicing in a CDK9-dependent manner. In NFAT5, promotes the introduction of alternative exon 4, which contains 2 stop codons and may target NFAT5 exon 4-containing transcripts to nonsense-mediated mRNA decay, leading to the down-regulation of NFAT5 protein. Affects splicing of mediators of steroid hormone signaling pathway, including kinases that phosphorylates ESR1, such as CDK2, MAPK1 and GSK3B, and transcriptional regulators, such as CREBBP, MED1, NCOR1 and NCOR2. By affecting GSK3B splicing, participates in ESR1 and AR stabilization. In myoblasts and epithelial cells, cooperates with HNRNPH1 to control the splicing of specific subsets of exons. In addition to binding mature mRNAs, also interacts with certain pri-microRNAs, including MIR663/miR-663a, MIR99B/miR-99b, and MIR6087/miR-6087. Binds pri-microRNAs on the 3' segment flanking the stem loop via the 5'-[ACG]CAUC[ACU]-3' consensus sequence. Required for the production of subsets of microRNAs, including MIR21 and MIR125B1. May be involved not only in microRNA primary transcript processing, but also stabilization (By similarity). Participates in MYC down-regulation at high cell density through the production of MYC-targeting microRNAs. Along with DDX5, may be involved in the processing of the 32S intermediate into the mature 28S ribosomal RNA. Promoter-specific transcription regulator, functioning as a coactivator or corepressor depending on the context of the promoter and the transcriptional complex in which it exists. Enhances NFAT5 transcriptional activity. Synergizes with TP53 in the activation of the MDM2 promoter; this activity requires acetylation on lysine residues. May also coactivate MDM2 transcription through a TP53-independent pathway. Coactivates MMP7 transcription. Along with CTNNB1, coactivates MYC, JUN, FOSL1 and cyclin D1/CCND1 transcription. Alone or in combination with DDX5 and/or SRA1 non-coding RNA, plays a critical role in promoting the assembly of proteins required for the formation of the transcription initiation complex and chromatin remodeling leading to coactivation of MYOD1-dependent transcription. This helicase-independent activity is required for skeletal muscle cells to properly differentiate into myotubes. During epithelial-to-mesenchymal transition, coregulates SMAD-dependent transcriptional activity, directly controlling key effectors of differentiation, including miRNAs which in turn directly repress its expression. Plays a role in estrogen and testosterone signaling pathway at several levels. Mediates the use of alternative promoters in estrogen-responsive genes and regulates transcription and splicing of a large number of steroid hormone target genes. Contrary to splicing regulation activity, transcriptional coregulation of the estrogen receptor ESR1 is helicase-independent. Plays a role in innate immunity. Specifically restricts bunyavirus infection, including Rift Valley fever virus (RVFV) or La Crosse virus (LACV), but not vesicular stomatitis virus (VSV), in an interferon- and DROSHA-independent manner. Binds to RVFV RNA, likely via structured viral RNA elements. Promotes mRNA degradation mediated by the antiviral zinc-finger protein ZC3HAV1, in an ATPase-dependent manner.
Classification
- Family (Pfam)
- PF00270 DEAD, PF00271 Helicase_C
- InterPro
- DDX17_ATP-bd-dom, DEAD/DEAH_box_helicase_dom, Helicase_ATP-bd, Helicase_C-like, P-loop_NTPase, RNA-helicase_DEAD-box_CS, RNA_helicase_DEAD_Q_motif
- Functional cluster
- DEAD-Box RNA Helicases & Biogenesis Factors
Experimental structures · PDB · 5
A predicted model is available from AlphaFold.
Gene Ontology · 31
- GO:0005737 cytoplasm
- GO:0005829 cytosol
- GO:0016020 membrane
- GO:0016607 nuclear speck
- GO:0005730 nucleolus
- GO:0005654 nucleoplasm
- GO:0005634 nucleus
- GO:1990904 ribonucleoprotein complex
- GO:0005524 ATP binding
- GO:0016887 ATP hydrolysis activity
- GO:0008186 ATP-dependent activity, acting on RNA
- GO:0003729 mRNA binding
- GO:0003723 RNA binding
- GO:0003724 RNA helicase activity
- GO:0003713 transcription coactivator activity
- GO:0000380 alternative mRNA splicing, via spliceosome
- GO:0030521 androgen receptor signaling pathway
- GO:0051607 defense response to virus
- GO:0006351 DNA-templated transcription
- GO:0001837 epithelial to mesenchymal transition
- GO:0030520 estrogen receptor signaling pathway
- GO:0002376 immune system process
- GO:0010586 miRNA metabolic process
- GO:0045445 myoblast differentiation
- GO:0045944 positive regulation of transcription by RNA polymerase II
- GO:0000381 regulation of alternative mRNA splicing, via spliceosome
- GO:2001014 regulation of skeletal muscle cell differentiation
- GO:0006357 regulation of transcription by RNA polymerase II
- GO:0031047 regulatory ncRNA-mediated gene silencing
- GO:0006396 RNA processing
- GO:0006364 rRNA processing
Neighborhood · nearest proteins
Related proteins · sequence + function similarity
- Probable ATP-dependent RNA helicase DDX17 0.96
- DEAD-box ATP-dependent RNA helicase 11 0.89
- Probable ATP-dependent RNA helicase DDX5 0.89
- Probable ATP-dependent RNA helicase DDX5 0.88
- Probable ATP-dependent RNA helicase DDX5 0.88
- Probable ATP-dependent RNA helicase DDX5 0.88
- DEAD-box ATP-dependent RNA helicase 30 0.88
- ATP-dependent RNA helicase dbp2 0.88
- ATP-dependent RNA helicase DBP2 0.88
- ATP-dependent RNA helicase dbp2 0.88
- DEAD-box ATP-dependent RNA helicase 52B 0.87
- ATP-dependent RNA helicase dbp2 0.87
Co-cited proteins · studied together in the literature
- Probable ATP-dependent RNA helicase DDX5 10 shared papers
- ATP-dependent RNA helicase p62 1 shared papers
- Probable ATP-dependent RNA helicase DDX17 2 shared papers
- Nuclear factor of activated T-cells 5 1 shared papers
- Zinc finger CCCH-type antiviral protein 1 2 shared papers
- Ribonuclease 3 1 shared papers
- Microprocessor complex subunit DGCR8 1 shared papers
- Core histone macro-H2A.1 1 shared papers
- Nuclear receptor coactivator 3 2 shared papers
- Probable ATP-dependent RNA helicase DDX5 1 shared papers
- Exosome complex component RRP40 2 shared papers
- Nuclear receptor coactivator 2 2 shared papers
Literature · 51 cited papers
- Site-specific mapping of the human SUMO proteome reveals co-modification with phosphorylation. Nat. Struct. Mol. Biol. · 2017
- The miRNA biogenesis factors, p72/DDX17 and KHSRP regulate the protein level of Ago2 in human cells. Biochim. Biophys. Acta · 2016
- Systematic determination of human cyclin dependent kinase (CDK)-9 interactome identifies novel functions in RNA splicing mediated by the DEAD box (DDX)-5/17 RNA helicases. Mol. Cell. Proteomics · 2015
- Identification of Novel Proteins Co-Purifying with Cockayne Syndrome Group B (CSB) Reveals Potential Roles for CSB in RNA Metabolism and Chromatin Dynamics. PLoS ONE · 2015
- SUMO-2 orchestrates chromatin modifiers in response to DNA damage. Cell Rep. · 2015
- System-wide analysis of SUMOylation dynamics in response to replication stress reveals novel small ubiquitin-like modified target proteins and acceptor lysines relevant for genome stability. Mol. Cell. Proteomics · 2015
- PMID 25452582 EMBO J. · 2014
- Uncovering global SUMOylation signaling networks in a site-specific manner. Nat. Struct. Mol. Biol. · 2014
- Stem-loop recognition by DDX17 facilitates miRNA processing and antiviral defense. Cell · 2014
- Mapping of SUMO sites and analysis of SUMOylation changes induced by external stimuli. Proc. Natl. Acad. Sci. U.S.A. · 2014
- RNA helicases DDX5 and DDX17 dynamically orchestrate transcription, miRNA, and splicing programs in cell differentiation. Cell Rep. · 2014
- Cell cycle-dependent regulation of Aurora kinase B mRNA by the Microprocessor complex. Biochem. Biophys. Res. Commun. · 2014
- … and 39 more in the literature graph