CDKN2A (cyclin dependent kinase 2a / p16)

2007-08-01   Raphael Saffroy  , Antoinette Lemoine  , Brigitte Debuire  

Laboratoire de Biochimie Biologie moléculaire, Hôpital Paul Brousse 94800 Villejuif, France

Identity

HGNC
LOCATION
9p21.3
IMAGE
Atlas Image
LEGEND
Probe(s) - Courtesy Mariano Rocchi, Resources for Molecular Cytogenetics
IMAGE
Atlas Image
LEGEND
CDKN2A (cyclin dependent kinase 2a / p16) Hybridization with Vysis CDKN2A/CEP 9 FISH Probe (Abbott Molecular, US) showing the CDKN2A gene on 9p21.3 (red signals) - Courtesy Adriana Zamecnikova.
LOCUSID
ALIAS
ARF,CDK4I,CDKN2,CMM2,INK4,INK4A,MLM,MTS-1,MTS1,P14,P14ARF,P16,P16-INK4A,P16INK4,P16INK4A,P19,P19ARF,TP16
FUSION GENES

DNA/RNA

Description

The gene encompasses 6.6 kb of DNA; 3 exons.

Transcription

471 nucleotides mRNA. The CDKN2 gene generates several transcript variants from different promoters. Each transcript differs in its first exon (E1), and utilizes alternate polyadenylation sites. E1-alpha, which is spliced into the common exons E2 and E3, gives rise to the p16-INK4 transcript. A putative DNA replication origin has been identified in close proximity of INK4/Arf locus that appears to transcriptionally repress p16 in a manner dependent on CDC6.

Proteins

Description

156 amino acids; 16.5 kDa protein.

Expression

Moderately expressed in many organs as thymus, liver, pancreas, prostate, lung, or kidney.

Function

P16-INK4a interacts strongly with cyclin-dependent kinase 4 and cyclin-dependent kinase 6 and inhibits their ability to interact with cyclins D. P16-INK4a induces cell cycle arrest at G1 and G2/M checkpoints, blocking them from phosphorylating RB1 and preventing exit from G1 phase of the cell cycle. P16-INK4a could act as a negative regulator of normal cells proliferation.

Homology

Belongs to the cdkn2 cyclin-dependent kinase inhibitor family.

Implicated in

Entity name
Cutaneous malignant melanoma 2 (CMM2)
Disease
Malignant melanoma arises de novo or from a preexisting benign nevus, which occurs most often in the skin but also may involve other sites.
Oncogenesis
Familial melanoma (comprising between 8 and 12% of all melanoma cases) is a genodermatosis transmitted as an autosomal dominant trait. CDKN2a has been identified as a major susceptibility gene for melanoma. However this gene accounts for a minority of familial melanoma. P16 is functionally inactivated by mutations or deletions, however, because many such mutations occur in exon 2, they can potentially also affect the alternative reading frame (ARF) protein.
Entity name
Familial atypical multiple mole melanoma carcinoma syndrome (FAMMM)
Disease
Patients with the FAMMM syndrome are genetically loaded with an increased risk of developing melanoma and other malignant neoplasms, for example, a pancreatic cancer.
Oncogenesis
FAMMM syndrome is an autosomal dominant disorder with variable incomplete penetrance of the clinical phenotypes. Germline mutations in the p16-INK4a gene were found in approximately 40% of the FAMMM syndrome.
Entity name
Sporadic cancer
Disease
Defects in CDKN2a are involved in tumor formation in a wide range of tissues.
Prognosis
Aberrant p16 expression is associated with more aggressive behavior.
Oncogenesis
LOH on 9p21 is one of the most frequent genetic alterations identified in human cancer. However, point mutations of p16 on the other chromosome are relatively rare. Promoter methylation appears as the commonest mechanism of p16 gene inactivation.
Entity name
Aging
Note
Expression of p16 increases markedly with aging in many human tissues. This finding has led to the proposal that p16 expression could be used as a biomarker of physiologic, as opposed to chronologic, age. It was suggested that an age-induced increase in p16 expression contributes to the decline of replicative potential of certain self-renewing compartments with aging.

Article Bibliography

Pubmed IDLast YearTitleAuthors

Other Information

Locus ID:

NCBI: 1029
MIM: 600160
HGNC: 1787
Ensembl: ENSG00000147889

Variants:

dbSNP: 1029
ClinVar: 1029
TCGA: ENSG00000147889
COSMIC: CDKN2A

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000147889ENST00000304494P42771
ENSG00000147889ENST00000304494K7PML8
ENSG00000147889ENST00000380151P42771
ENSG00000147889ENST00000479692K7ENC6
ENSG00000147889ENST00000494262P42771
ENSG00000147889ENST00000497750K7ES20
ENSG00000147889ENST00000498124P42771
ENSG00000147889ENST00000498628P42771
ENSG00000147889ENST00000530628Q8N726
ENSG00000147889ENST00000578845P42771
ENSG00000147889ENST00000579122J3QRG6
ENSG00000147889ENST00000579755Q8N726

Expression (GTEx)

0
5
10
15
20

Pathways

PathwaySourceExternal ID
Cell cycleKEGGko04110
p53 signaling pathwayKEGGko04115
Pancreatic cancerKEGGko05212
GliomaKEGGko05214
MelanomaKEGGko05218
Bladder cancerKEGGko05219
Chronic myeloid leukemiaKEGGko05220
Non-small cell lung cancerKEGGko05223
Cell cycleKEGGhsa04110
p53 signaling pathwayKEGGhsa04115
Pathways in cancerKEGGhsa05200
Pancreatic cancerKEGGhsa05212
GliomaKEGGhsa05214
MelanomaKEGGhsa05218
Bladder cancerKEGGhsa05219
Chronic myeloid leukemiaKEGGhsa05220
Non-small cell lung cancerKEGGhsa05223
HTLV-I infectionKEGGko05166
HTLV-I infectionKEGGhsa05166
Viral carcinogenesisKEGGhsa05203
Viral carcinogenesisKEGGko05203
MicroRNAs in cancerKEGGhsa05206
MicroRNAs in cancerKEGGko05206
Metabolism of proteinsREACTOMER-HSA-392499
Post-translational protein modificationREACTOMER-HSA-597592
SUMOylationREACTOMER-HSA-2990846
SUMO E3 ligases SUMOylate target proteinsREACTOMER-HSA-3108232
SUMOylation of DNA damage response and repair proteinsREACTOMER-HSA-3108214
Gene ExpressionREACTOMER-HSA-74160
Generic Transcription PathwayREACTOMER-HSA-212436
Transcriptional Regulation by TP53REACTOMER-HSA-3700989
Cell CycleREACTOMER-HSA-1640170
Cell Cycle, MitoticREACTOMER-HSA-69278
Mitotic G1-G1/S phasesREACTOMER-HSA-453279
G1 PhaseREACTOMER-HSA-69236
Cyclin D associated events in G1REACTOMER-HSA-69231
Cellular responses to stressREACTOMER-HSA-2262752
Cellular SenescenceREACTOMER-HSA-2559583
Oncogene Induced SenescenceREACTOMER-HSA-2559585
Oxidative Stress Induced SenescenceREACTOMER-HSA-2559580
Senescence-Associated Secretory Phenotype (SASP)REACTOMER-HSA-2559582
SUMOylation of transcription factorsREACTOMER-HSA-3232118
Regulation of TP53 ActivityREACTOMER-HSA-5633007
Regulation of TP53 Expression and DegradationREACTOMER-HSA-6806003
Regulation of TP53 DegradationREACTOMER-HSA-6804757
Platinum drug resistanceKEGGko01524
Endocrine resistanceKEGGko01522
Platinum drug resistanceKEGGhsa01524
Endocrine resistanceKEGGhsa01522

Protein levels (Protein atlas)

Not detected
Low
Medium
High

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA446155Precursor Cell Lymphoblastic Leukemia-LymphomaDiseaseMultilinkAnnotationassociated26104880

References

Pubmed IDYearTitleCitations
372118402024LncRNA CAI2 Contributes to Poor Prognosis of Glioma through the PI3K-Akt Signaling Pathway.0
375780682024ARID5B, IKZF1, GATA3, CEBPE, and CDKN2A germline polymorphisms and predisposition to childhood acute lymphoblastic leukemia.0
378612072024Human papillomavirus and p16(INK4a) in oropharyngeal squamous cell carcinomas: A systematic review and meta-analysis.0
379245302024Prognosis of CDKN2A germline mutation in patients with familial melanoma: a systematic review and meta-analysis.0
380978742024FISH analysis reveals CDKN2A and IFNA14 co-deletion is heterogeneous and is a prominent feature of glioblastoma.0
382657482024CDKN2A/B deletion in IDH-mutant astrocytomas: An evaluation by Fluorescence in-situ hybridization.0
384217072024METTL14-Mediated m6a Modification of CDKN2A Promotes the Development of Retinoblastoma by Inhibiting the p53 Pathway.1
384387732024CDKN2A promoter methylation enhances self-renewal of glioblastoma stem cells and confers resistance to carmustine.1
384415302024PR55α-controlled protein phosphatase 2A inhibits p16 expression and blocks cellular senescence induction by γ-irradiation.0
384572262024Treatments, prognostic factors, and genetic heterogeneity in advanced cholangiocarcinoma: A multicenter real-world study.1
385001582024HPV related p16(INK4A) and HSV in benign and potentially malignant oral mucosa pathologies.0
385460682024High P16INK4A Expression, Keratinizing Features, and Surgical Margin-Free Status are Associated with Improved Survival in Patients with Oral Squamous Cell Carcinomas.0
386263412024De Novo Purine Metabolism is a Metabolic Vulnerability of Cancers with Low p16 Expression.0
386271952024iChIP-SILAC analysis identifies epigenetic regulators of CpG methylation of the p16(INK4A) gene.0
386309112024Uterine Inflammatory Myofibroblastic Tumors: p16 as a Surrogate for CDKN2A Deletion and Predictor of Aggressive Behavior.0

Citation

Raphael Saffroy ; Antoinette Lemoine ; Brigitte Debuire

CDKN2A (cyclin dependent kinase 2a / p16)

Atlas Genet Cytogenet Oncol Haematol. 2007-08-01

Online version: http://atlasgeneticsoncology.org/gene/146/gene-fusions-explorer/css/teaching-explorer/

Historical Card

2004-08-01 CDKN2A (cyclin dependent kinase 2a / p16) by  Raphael Saffroy,Antoinette Lemoine,Brigitte Debuire 

Laboratoire de Biochimie Biologie moléculaire, Hôpital Paul Brousse 94800 Villejuif, France