PLK2 (Polo Like Kinase 2) Gene

A serine/threonine-protein kinase involved in cell cycle regulation, centriole duplication, and synaptic plasticity.

Gene Information Card

Symbol PLK2
Full Name Polo Like Kinase 2
Gene Type Protein coding
Chromosomal Location 5q11.2
NCBI Gene ID 10769 ncbi.nlm.nih.gov/gene/10769
Ensembl ID ENSG00000145632
UniProt ID Q9NYY3
OMIM ID 607023
HGNC ID 9077
Aliases SNK, hPlk2, polo-like kinase 2

Description

PLK2 (Polo Like Kinase 2) encodes a serine/threonine-protein kinase belonging to the CDC5/Polo subfamily. It is involved in cell cycle progression, particularly in centriole duplication and mitotic entry. PLK2 also plays roles in synaptic plasticity, neuronal differentiation, and response to DNA damage. Its expression is regulated in a cell cycle-dependent manner and is frequently altered in various cancers and neurological disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (multiple types) Dysregulation of PLK2 expression and activity contributes to uncontrolled cell proliferation and genomic instability. COSMIC; NCBI Gene
Neurodegenerative disorders (e.g., Alzheimer's disease) PLK2 modulates tau phosphorylation and synaptic function; altered expression linked to pathology. NCBI Gene; UniProt
Developmental disorders Rare variants in PLK2 have been associated with intellectual disability and microcephaly. ClinVar; OMIM

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.5 Medium
Testis 8.3 Medium
Lymph node 6.1 Low
Liver 2.4 Low
Heart 1.8 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 15.2 High expression in cervical cancer cell line
HEK293 10.1 Moderate expression in embryonic kidney cells
SH-SY5Y 18.7 High expression in neuroblastoma cell line
MCF7 7.5 Moderate expression in breast cancer cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1012C>T (p.Arg338Trp) Missense <0.01% Unknown; reported in ClinVar as variant of uncertain significance
c.1456G>A (p.Glu486Lys) Missense <0.01% Unknown; reported in ClinVar as variant of uncertain significance
c.1789_1790insA (p.Thr597Asnfs*5) Frameshift <0.01% Predicted loss of function; reported in COSMIC
Mutation functional classification

Loss of Function (LOF)

Frameshift and nonsense mutations in PLK2 are predicted to result in truncated or absent protein, leading to loss of kinase activity and impaired centriole duplication.

Gain of Function (GOF)

Missense mutations in the kinase domain may increase catalytic activity, potentially driving oncogenic signaling; however, specific gain-of-function variants are not well characterized.

Dominant Negative (DN)

Certain missense mutations in the polo-box domain may interfere with substrate binding and exert dominant-negative effects on cell cycle regulation.

Pathways

• Cell Cycle (Reactome: R-HSA-1640170)
• Mitotic G1-G1/S phases (Reactome: R-HSA-453279)
• Centrosome maturation (Reactome: R-HSA-380270)
• PLK2-mediated phosphorylation of tau (UniProt)

Protein Summary

PLK2 is a 685-amino acid serine/threonine kinase with an N-terminal kinase domain and a C-terminal polo-box domain. It localizes to centrosomes and is essential for centriole duplication. PLK2 phosphorylates substrates such as CEP192, CEP152, and tau. Its activity is tightly regulated during the cell cycle, and it is implicated in tumor suppression and neuronal function.

Related Products

Product name Cat.No. Species Gene ID
PLK2 Knockout HEK293 Cell Line EDJ-KQ1537 Human 10769 Details Get a Quote
PLK2 Knockout A-549 Cell Line EDJ-KQ21198 Human 10769 Details Get a Quote
PLK2 Knockout HCT 116 Cell Line EDJ-KQ21199 Human 10769 Details Get a Quote
PLK2 Knockout HeLa Cell Line EDJ-KQ21200 Human 10769 Details Get a Quote
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