CCNT2: Cyclin T2

A regulatory subunit of the P-TEFb complex involved in transcriptional elongation and cell cycle control.

Gene Information Card

Symbol CCNT2
Full Name Cyclin T2
Gene Type Protein coding
Chromosomal Location 2q21.3
NCBI Gene ID 905 ncbi.nlm.nih.gov/gene/905
Ensembl ID ENSG00000115947
UniProt ID O60583
OMIM ID 603862
HGNC ID 1600
Aliases CYCT2, cyclin T2a, cyclin T2b

Description

CCNT2 encodes cyclin T2, a regulatory subunit of the positive transcription elongation factor b (P-TEFb) complex. P-TEFb, composed of cyclin T2 and CDK9, phosphorylates the C-terminal domain of RNA polymerase II to promote transcriptional elongation. Cyclin T2 is involved in cell cycle regulation, differentiation, and viral replication, particularly HIV-1 Tat-mediated transactivation. Alternative splicing generates isoforms T2a and T2b.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
HIV-1 infection CCNT2 is a critical cofactor for HIV-1 Tat protein, which recruits P-TEFb to the viral promoter to enhance transcription elongation. PMID: 10523660
Breast cancer Overexpression of CCNT2 is associated with poor prognosis and may promote tumor progression by dysregulating transcriptional elongation. PMID: 25636838
Colorectal cancer CCNT2 upregulation correlates with increased proliferation and metastasis, potentially via CDK9-mediated transcription of oncogenes. PMID: 29367608

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 15.2 Medium
Lymph node 12.8 Medium
Bone marrow 11.5 Medium
Spleen 10.9 Medium
Brain 6.3 Low
Cell Line Expression
Cell Line nTPM Notes
HEK 293 18.5 High expression
HeLa 14.2 High expression
K562 12.0 Medium expression
MCF7 10.1 Medium expression
HepG2 8.7 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1123G>A (p.Gly375Arg) Missense <0.01% (gnomAD) Unknown; predicted to affect protein stability
c.1456C>T (p.Arg486Trp) Missense <0.01% (gnomAD) Unknown; located in cyclin domain
c.1789_1790insA (p.Thr597Asnfs*12) Frameshift <0.01% (COSMIC) Loss of function; truncation of C-terminal region
Mutation functional classification

Loss of Function (LOF)

Frameshift mutations leading to premature stop codons (e.g., p.Thr597Asnfs*12) are predicted to cause loss of function by disrupting CDK9 binding or P-TEFb complex assembly.

Gain of Function (GOF)

No well-characterized gain-of-function mutations have been reported for CCNT2.

Dominant Negative (DN)

No dominant-negative mutations have been described for CCNT2.

Pathways

P-TEFb complex (Reactome: R-HSA-167162)
HIV-1 transcription elongation (Reactome: R-HSA-167243)
RNA polymerase II transcription elongation (Reactome: R-HSA-75955)

Protein Summary

Cyclin T2 is a 726-amino acid protein (isoform 1) that contains a cyclin N-terminal domain and a C-terminal PEST sequence. It forms a heterodimer with CDK9 to constitute the P-TEFb complex. The cyclin T2/CDK9 complex phosphorylates serine 2 of the RNA polymerase II C-terminal domain, enabling efficient transcriptional elongation. Cyclin T2 also interacts with the HIV-1 Tat protein to facilitate viral transcription. Two major isoforms exist: T2a (full-length) and T2b (lacking exon 7).

Related Products

Product name Cat.No. Species Gene ID
CCNT2 Knockout HEK293 Cell Line EDJ-KQ3510 Human 905 Details Get a Quote
CCNT2 Knockout A-549 Cell Line EDJ-KQ25323 Human 905 Details Get a Quote
CCNT2 Knockout HCT 116 Cell Line EDJ-KQ25324 Human 905 Details Get a Quote
CCNT2 Knockout HeLa Cell Line EDJ-KQ25325 Human 905 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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