Tag Content
SG ID
SG00004951 
UniProt Accession
Theoretical PI
9.06  
Molecular Weight
69290 Da  
Genbank Nucleotide ID
Genbank Protein ID
Gene Name
Ddx5 
Gene Synonyms/Alias
Tnz2 
Protein Name
Probable ATP-dependent RNA helicase DDX5 
Protein Synonyms/Alias
EC=3.6.4.13 DEAD box RNA helicase DEAD1;mDEAD1 DEAD box protein 5; RNA helicase p68; 
Organism
Mus musculus (Mouse) 
NCBI Taxonomy ID
10090 
Chromosome Location
chr:11;106641669-106650499;-1
View in Ensembl genome browser  
Function in Stage
Uncertain 
Function in Cell Type
Uncertain 
Probability (GAS) of Function in Spermatogenesis
0.909156707 
The probability was calculated by GAS algorithm, ranging from 0 to 1. The closer it is to 1, the more possibly it functions in spermatogenesis.
Description
Temporarily unavailable 
Abstract of related literatures
1. The complete cDNA coding for mouse P68 RNA helicase was cloned and its nucleotide sequence was determined. The sequence is about 95% identical to the human equivalent. Whereas the 5'-untranslated region is less conserved (71%), the 3'-ends of mouse and human mRNAs are nearly identical. Between stop codon and poly(A)-tail both sequences are 97% conserved. At the level of amino acid sequence, the similarity of both, mouse and human, DEAD box family proteins is as high as 98%. In situ hybridizations using cDNA subfragments as probes revealed a testis-selective expression of P68 RNA helicase mRNA. The signal was restricted to late pachytene spermatocytes and haploid spermatids. Northern blot analyses corroborated these results but suggested that expression of related mRNA species occurs in a variety of other tissues. PMID: [8445986] 

2. The mouse (Mus musculus) is the premier animal model for understanding human disease and development. Here we show that a comprehensive understanding of mouse biology is only possible with the availability of a finished, high-quality genome assembly. The finished clone-based assembly of the mouse strain C57BL/6J reported here has over 175,000 fewer gaps and over 139 Mb more of novel sequence, compared with the earlier MGSCv3 draft genome assembly. In a comprehensive analysis of this revised genome sequence, we are now able to define 20,210 protein-coding genes, over a thousand more than predicted in the human genome (19,042 genes). In addition, we identified 439 long, non-protein-coding RNAs with evidence for transcribed orthologs in human. We analyzed the complex and repetitive landscape of 267 Mb of sequence that was missing or misassembled in the previously published assembly, and we provide insights into the reasons for its resistance to sequencing and assembly by whole-genome shotgun approaches. Duplicated regions within newly assembled sequence tend to be of more recent ancestry than duplicates in the published draft, correcting our initial understanding of recent evolution on the mouse lineage. These duplicates appear to be largely composed of sequence regions containing transposable elements and duplicated protein-coding genes; of these, some may be fixed in the mouse population, but at least 40% of segmentally duplicated sequences are copy number variable even among laboratory mouse strains. Mouse lineage-specific regions contain 3,767 genes drawn mainly from rapidly-changing gene families associated with reproductive functions. The finished mouse genome assembly, therefore, greatly improves our understanding of rodent-specific biology and allows the delineation of ancestral biological functions that are shared with human from derived functions that are not. PMID: [19468303] 

3. The ability of macrophages to clear pathogens and elicit a sustained immune response is regulated by various cytokines, including interferon-gamma (IFN-gamma). To investigate the molecular mechanisms by which IFN-gamma modulates phagosome functions, we profiled the changes in composition, abundance, and phosphorylation of phagosome proteins in resting and activated macrophages by using quantitative proteomics and bioinformatics approaches. We identified 2415 phagosome proteins together with 2975 unique phosphorylation sites with a high level of sensitivity. Using network analyses, we determined that IFN-gamma delays phagosomal acquisition of lysosomal hydrolases and peptidases for the gain of antigen presentation. Furthermore, this gain in antigen presentation is dependent on phagosomal networks of the actin cytoskeleton and vesicle-trafficking proteins, as well as Src kinases and calpain proteases. Major histocompatibility complex class I antigen-presentation assays validated the molecular participation of these networks in the enhanced capacity of IFN-gamma-activated macrophages to crosspresent exogenous antigens to CD8(+) T cells. PMID: [19144319] 

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Function
Involved in the alternative regulation of pre-mRNAsplicing; its RNA helicase activity is necessary for increasingtau exon 10 inclusion and occurs in a RBM4-dependent manner. Bindsto the tau pre-mRNA in the stem-loop region downstream of exon 10.The rate of ATP hydrolysis is highly stimulated by single-strandedRNA. Involved in transcriptional regulation; the function isindependent of the RNA helicase activity. Transcriptionalcoactivator for estrogen receptor ESR1 and androgen receptor AR.Increases ESR1 AF-1 domain-mediated transactivation and ESR1 AF-1and AF-2 domains transcriptional synergistic activity. Synergizeswith DDX17 and SRA1 RNA to activate MYOD1 transcriptional activityand involved in skeletal muscle differentiation. Transcriptionalcoactivator for p53/TP53 and involved in p53/TP53 transcriptionalresponse to DNA damage and p53/TP53-dependent apoptosis.Transcriptional coactivator for RUNX2 and involved in regulationof osteoblast differentiation. Acts as transcriptional repressorin a promoter-specicic manner; the function probbaly involvesassociation with histone deacetylases, such as HDAC1. 
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Subcellular Location
Nucleus, nucleolus (By similarity). 
Tissue Specificity
 
Gene Ontology
GO IDGO termEvidence
GO:0005730 C:nucleolus ISS:UniProtKB.
GO:0030529 C:ribonucleoprotein complex ISO:MGI.
GO:0005681 C:spliceosomal complex IEA:UniProtKB-KW.
GO:0005524 F:ATP binding IEA:UniProtKB-KW.
GO:0008026 F:ATP-dependent helicase activity IEA:InterPro.
GO:0003723 F:RNA binding IEA:UniProtKB-KW.
GO:0003724 F:RNA helicase activity ISS:UniProtKB.
GO:0003713 F:transcription coactivator activity ISS:UniProtKB.
GO:0001701 P:in utero embryonic development IMP:MGI.
GO:0006397 P:mRNA processing IEA:UniProtKB-KW.
GO:0000122 P:negative regulation of transcription from RNA polymerase II promoter ISS:UniProtKB.
GO:0043517 P:positive regulation of DNA damage response, signal transduction by p53 class mediator ISS:UniProtKB.
GO:0045944 P:positive regulation of transcription from RNA polymerase II promoter ISS:UniProtKB.
GO:0000381 P:regulation of alternative nuclear mRNA splicing, via spliceosome ISS:UniProtKB.
GO:0060765 P:regulation of androgen receptor signaling pathway ISS:UniProtKB.
GO:0045667 P:regulation of osteoblast differentiation IMP:UniProtKB.
GO:2001014 P:regulation of skeletal muscle cell differentiation IMP:UniProtKB.
GO:0008380 P:RNA splicing IEA:UniProtKB-KW.
GO:0072332 P:signal transduction by p53 class mediator resulting in induction of apoptosis ISS:UniProtKB.
GO:0006351 P:transcription, DNA-dependent IEA:UniProtKB-KW.
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Interpro
IPR011545;    DNA/RNA_helicase_DEAD/DEAH_N.
IPR014001;    Helicase_ATP-bd.
IPR001650;    Helicase_C.
IPR012587;    P68HR.
IPR000629;    RNA-helicase_DEAD-box_CS.
IPR014014;    RNA_helicase_DEAD_Q_motif.
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Pfam
PF00270;    DEAD;    1.
PF00271;    Helicase_C;    1.
PF08061;    P68HR;    2.
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SMART
SM00487;    DEXDc;    1.
SM00490;    HELICc;    1.
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PROSITE
PS00039;    DEAD_ATP_HELICASE;    1.
PS51192;    HELICASE_ATP_BIND_1;    1.
PS51194;    HELICASE_CTER;    1.
PS51195;    Q_MOTIF;    1.
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PRINTS
Created Date
18-Oct-2012 
Record Type
GAS predicted 
Sequence Annotation
CHAIN         1    614       Probable ATP-dependent RNA helicase DDX5.
                             /FTId=PRO_0000054992.
DOMAIN      125    300       Helicase ATP-binding.
DOMAIN      328    475       Helicase C-terminal.
NP_BIND     114    116       ATP (By similarity).
NP_BIND     138    145       ATP (By similarity).
REGION      477    614       Transactivation domain (By similarity).
MOTIF        94    122       Q motif.
MOTIF       248    251       DEAD box.
BINDING     121    121       ATP (By similarity).
MOD_RES       6      6       Phosphoserine (By similarity).
MOD_RES      30     30       Phosphoserine (By similarity).
MOD_RES      32     32       N6-acetyllysine (By similarity).
MOD_RES      33     33       N6-acetyllysine (By similarity).
MOD_RES      40     40       N6-acetyllysine (By similarity).
MOD_RES     202    202       Phosphotyrosine (By similarity).
MOD_RES     297    297       Phosphotyrosine (By similarity).
MOD_RES     480    480       Phosphoserine.
MOD_RES     502    502       Omega-N-methylated arginine (By
                             similarity).
MOD_RES     507    507       Phosphothreonine (By similarity).
CROSSLNK     53     53       Glycyl lysine isopeptide (Lys-Gly)
                             (interchain with G-Cter in SUMO) (By
                             similarity).
CONFLICT    112    112       Q -> H (in Ref. 1; CAA46581).
CONFLICT    159    159       Q -> H (in Ref. 1; CAA46581).
CONFLICT    597    597       L -> V (in Ref. 1; CAA46581).
CONFLICT    600    600       A -> P (in Ref. 1; CAA46581).
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Nucleotide Sequence
Length: 2318 bp   Go to nucleotide: FASTA
Protein Sequence
Length: 614 bp   Go to amino acid: FASTA
The verified Protein-Protein interaction information
UniProt
Gene Symbol Ref Databases
YwhabIntAct 
AireIntAct 
BtkMINT 
BtkIntAct 
IkbkbIntAct 
Tial1MINT 
Other Protein-Protein interaction resources
String database  
View Microarray data
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