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PPP1R13L (protein phosphatase 1, regulatory (inhibitor) subunit 13 like)

Identity

Other namesRAI (relA associated inhibitor)
IASPP (Inhibitor of ASPP protein)
Hugo PPP1R13L
Location 19q13.32

DNA/RNA

Description 26,674 bp 13 exons.
Transcription 3,076 bps.

Protein

Description 828 amino acids.
Function PPP1R13L was originally named RAI, an acronym for RelA associated inhibitor. It was originally identified by yeast two-hybrid screening using RelA as bait. PPP1R13L was shown to associate specifically with relA and inhibit relA mediated NF-kappaB activated transcription when NF-kappaB specific transcription was activated by TNF. Yang et al. found no interaction with p53. The mRNA expression was examined in several tissues and was found to be high in heart, placenta, prostate tissues and detectable in lung, kidney, pancreas, spleen thymus, ovary, small intestine and colon. Bergamaschi et al found that PPP1R13L interacts with p53. Antisense RNA or RNAi mediated down regulation of PPP1R13L expression and induced apoptosis. Increased expression of PPP1R13L lead to increased resistance towards cisplatin and UV-induced apoptosis. This indicates that RAI inhibits apoptosis.
Several studies provide evidence that PPP1R13L expression is increased in tumor tissue. In a study of colorectal adenomas and colorectal cancers, PPP1R13L expression was found to be substantially higher in lesions than in the normal tissue from the same patient. PPP1R13L expression has also been found to be increased in breast carcinomas and in blood cells in patients with acute leukemia.
In a prospective study of lung cancer among 265 lung cancer cases and 272 controls nested within the population based 'Diet, Cancer and Health study', PPP1R13L expression in mononuclear blood cells (isolated by buffy coat) was not associated with risk of lung cancer. mRNA levels were found to be 41% higher in women than in men.

Mutations

Note Genetic Epidemiology:
The most frequently studied polymorphism in PPP1R13L is PPP1R13L IVS1 A4364G (rs1970764). Carriers of the variant allele have been shown to be at decreased risk of basal cell carcinoma among younger persons (< 50 years), breast cancer (<55 years) and lung cancer (<56 years).
The polymorphism is part of a haplotype, which has a stronger association with risk of cancer than the polymorphism itself. Homozygous carriers of the haplotype ERCC1 Asn118AsnA, ASE-1 G-21AG, PPP1R13L IVS1 A4364GA have been shown to be at increased risk of breast cancer and lung cancer. Thus, women who were homozygous carriers of the haplotype ERCC1 Asn118AsnA, ASE-1 G-21AG, RAI IVS1 A4364GA, had a 9.5-fold higher risk of breast cancer before 55 years of age than women who were not homozygous carriers of the haplotype. Older women and heterozygous carriers were not at an increased risk of breast cancer. Homozygous carriers of the haplotype were found to be at 4.9-fold increased risk of lung cancer in the age interval 50-55 years. The association was stronger among women than among men, although the difference was not statistically significant. In subsequent study including more cases and a larger comparison group, a statistically significant difference between genders was found. Furthermore, it was found that the haplotype interacts with smoking intensity. Thus, among women, who were carriers of the haplotype, additional smoking at high smoking intensity (>20 cigarettes/day) was associated with increased lung cancer risk. This was not seen among women who were not homozygous carriers of the haplotype or among men.
The haplotype was not associated with risk of testis cancer or with risk of colorectal adenomas or colorectal cancer. Furthermore, the haplotype was not associated with risk of basal cell carcinoma among older persons (>60 years).
These results indicate that the haplotype may be associated with risk of cancer primarily among young and middle aged persons and that it may be specific for women.

Implicated in

Entity General increased cancer risk
Note No human disease has been linked to inactivation of PPP1R13L. However, polymorphisms in PPP1R13L may be associated with increased cancer risk (see above).
  

External links

Nomenclature
HugoPPP1R13L
GDBPPP1R13L
Entrez_GenePPP1R13L  10848  protein phosphatase 1, regulatory (inhibitor) subunit 13 like
Cards
AtlasPPP1R13LID42997ch19q13
GeneCardsPPP1R13L
EnsemblPPP1R13L [Search_View]   ENSG00000104881 [Gene_View]
GenatlasPPP1R13L
GeneLynxPPP1R13L
eGenomePPP1R13L
euGene10848
Genomic and cartography
GoldenPathPPP1R13L  -  19q13.32   chr19:50574739-50600129 -  19q13.32   [Description]    (hg18-Mar_2006)
EnsemblPPP1R13L - 19q13.32 [CytoView]
NCBIMapview
OMIMDisease map [OMIM]
HomoloGenePPP1R13L
Gene and transcription
GenbankAF078036 [ ENTREZ ]
GenbankAF078037 [ ENTREZ ]
GenbankAJ888472 [ ENTREZ ]
GenbankAK130326 [ ENTREZ ]
GenbankAY869712 [ ENTREZ ]
RefSeqNM_006663 [ SRS ]    NM_006663 [ ENTREZ ]
RefSeqAC_000062 [ SRS ]    AC_000062 [ ENTREZ ]
RefSeqNC_000019 [ SRS ]    NC_000019 [ ENTREZ ]
RefSeqNT_011109 [ SRS ]    NT_011109 [ ENTREZ ]
RefSeqNW_927217 [ SRS ]    NW_927217 [ ENTREZ ]
AceViewPPP1R13L AceView - NCBI
UnigeneHs.466937 [ SRS ]    Hs.466937 [ NCBI ]     HS466937 [ spliceNest ]
Fast-db13365 (alternative variants)
Protein : pattern, domain, 3D structure
SwissProtQ8WUF5 [ SRS]    Q8WUF5 [ EXPASY ]     Q8WUF5 [ INTERPRO ]
PrositePS50297 ANK_REP_REGION [ SRS ]    PS50297 ANK_REP_REGION [ Expasy ]
PrositePS50088 ANK_REPEAT [ SRS ]    PS50088 ANK_REPEAT [ Expasy ]
PrositePS50002 SH3 [ SRS ]    PS50002 SH3 [ Expasy ]
InterproIPR002110 ANK [ SRS ]    IPR002110 ANK [ EBI ]
InterproIPR001452 SH3 [ SRS ]    IPR001452 SH3 [ EBI ]
CluSTrQ8WUF5
PfamPF00023 Ank [ SRS ]    PF00023 Ank [ Sanger ]    pfam00023 [ NCBI-CDD ]
PfamPF00018 SH3_1 [ SRS ]    PF00018 SH3_1 [ Sanger ]    pfam00018 [ NCBI-CDD ]
SmartSM00248 ANK [EMBL]
SmartSM00326 SH3 [EMBL]
ProdomPD000066 SH3[INRA-Toulouse]
ProdomQ8WUF5 IASPP_HUMAN [ Domain structure ]   Q8WUF5 IASPP_HUMAN  [ sequences sharing at least 1 domain ]
BlocksQ8WUF5
HPRD09195
Protein Interaction databases
DIPQ8WUF5
IntActQ8WUF5
Polymorphism : SNP, mutations, diseases
OMIM607463    [ map ]   
GENECLINICS607463
SNPPPP1R13L [dbSNP-NCBI]  
SNPNM_006663 [SNP-NCI]  
SNPPPP1R13L [GeneSNPs - Utah]  PPP1R13L] [HGBASE - SRS]
HAPMAPPPP1R13L [HAPMAP]  
HGMDPPP1R13L
General knowledge
Family BrowserPPP1R13L [UCSC Family Browser]
SOURCENM_006663
SMDHs.466937
SAGEHs.466937
GOtranscription corepressor activity [Amigo]  transcription corepressor activity
GOnucleus [Amigo]  nucleus
GOcytoplasm [Amigo]  cytoplasm
GOtranscription [Amigo]  transcription
GOregulation of transcription, DNA-dependent [Amigo]  regulation of transcription, DNA-dependent
GOapoptosis [Amigo]  apoptosis
GOtranscription factor binding [Amigo]  transcription factor binding
PubGenePPP1R13L
TreeFamPPP1R13L
CTD10848 [Comparative ToxicoGenomics Database]
Other databases
Probes
ProbePPP1R13L Related clones (RZPD - Berlin)
PubMed
PubMed17 Pubmed reference(s) in LocusLink

Bibliography

Identification of a novel inhibitor of nuclear factor-kappaB, RelA-associated inhibitor.
Yang JP, Hori M, Sanda T, Okamoto T
The Journal of biological chemistry. 1999 ; 274 (22) : 15662-15670.
PMID 10336463
 
Multiple single nucleotide polymorphisms on human chromosome 19q13.2-3 associate with risk of Basal cell carcinoma.
Yin J, Rockenbauer E, Hedayati M, Jacobsen NR, Vogel U, Grossman L, Bolund L, Nexˆ½ BA
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2002 ; 11 (11) : 1449-1453.
PMID 12433725
 
iASPP oncoprotein is a key inhibitor of p53 conserved from worm to human.
Bergamaschi D, Samuels Y, O'Neil NJ, Trigiante G, Crook T, Hsieh JK, O'Connor DJ, Zhong S, Campargue I, Tomlinson ML, Kuwabara PE, Lu X
Nature genetics. 2003 ; 33 (2) : 162-167.
PMID 12524540
 
A specific haplotype of single nucleotide polymorphisms on chromosome 19q13.2-3 encompassing the gene RAI is indicative of post-menopausal breast cancer before age 55.
Nexˆ½ BA, Vogel U, Olsen A, Ketelsen T, Bukowy Z, Thomsen BL, Wallin H, Overvad K, Tjˆ½nneland A
Carcinogenesis. 2003 ; 24 (5) : 899-904.
PMID 12771034
 
Two regions in chromosome 19q13.2-3 are associated with risk of lung cancer.
Vogel U, Laros I, Jacobsen NR, Thomsen BL, Bak H, Olsen A, Bukowy Z, Wallin H, Overvad K, Tjˆ½nneland A, Nexˆ½ BA, Raaschou-Nielsen O
Mutation research. 2004 ; 546 (1-2) : 65-74.
PMID 14757194
 
Polymorphisms in RAI and in genes of nucleotide and base excision repair are not associated with risk of testicular cancer.
Laska MJ, Nexˆ½ BA, Vistisen K, Poulsen HE, Loft S, Vogel U
Cancer letters. 2005 ; 225 (2) : 245-251.
PMID 15885892
 
Effect of polymorphisms in XPD, RAI, ASE-1 and ERCC1 on the risk of basal cell carcinoma among Caucasians after age 50.
Vogel U, Olsen A, Wallin H, Overvad K, Tjˆ½nneland A, Nexˆ½ BA
Cancer detection and prevention. 2005 ; 29 (3) : 209-214.
PMID 15936590
 
The expression of iASPP in acute leukemias.
Zhang X, Wang M, Zhou C, Chen S, Wang J
Leukemia research. 2005 ; 29 (2) : 179-183.
PMID 15607367
 
Clinical management of women with metastatic breast cancer: a descriptive study according to age group.
Manders K, van de Poll-Franse LV, Creemers GJ, Vreugdenhil G, van der Sangen MJ, Nieuwenhuijzen GA, Roumen RM, Voogd AC
BMC cancer. 2006 ; 6 : page 179.
PMID 16824210
 
Clinical management of women with metastatic breast cancer: a descriptive study according to age group.
Manders K, van de Poll-Franse LV, Creemers GJ, Vreugdenhil G, van der Sangen MJ, Nieuwenhuijzen GA, Roumen RM, Voogd AC
BMC cancer. 2006 ; 6 : page 179.
PMID 16824210
 
ERCC1, XPD and RAI mRNA levels in lymphocytes are not associated with lung cancer risk in a prospective study of Danes.
Vogel U, Nexˆ½ BA, Tjˆ½nneland A, Wallin H, Hertel O, Raaschou-Nielsen O
Mutation research. 2006 ; 593 (1-2) : 88-96.
PMID 16054657
 
Gene-environment interactions between smoking and a haplotype of RAI, ASE-1 and ERCC1 polymorphisms among women in relation to risk of lung cancer in a population-based study.
Vogel U, Sˆ½rensen M, Hansen RD, Tjˆ½nneland A, Overvad K, Wallin H, Nexˆ½ BA, Raaschou-Nielsen O
Cancer letters. 2007 ; 247 (1) : 159-165.
PMID 16690207
 
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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Contributor(s)

Written12-2006Ulla Vogel

Citation

This paper should be referenced as such :
Vogel U . PPP1R13L (protein phosphatase 1, regulatory (inhibitor) subunit 13 like). Atlas Genet Cytogenet Oncol Haematol. December 2006 .
URL : http://AtlasGeneticsOncology.org/Genes/PPP1R13LID42997ch19q13.html

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Wed Jul 2 08:26:10 2008


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