Target intelligence / Profile preview

Protein PAT1 homolog 2 (PATL2)

Target
PATL2
Molecular classification
RNA-binding protein, mRNA decapping activator, transcriptional regulator, translational repressor, processing body (P-body) component
01

Overview

Protein PAT1 homolog 2 (**PATL2**) is a highly conserved RNA-binding protein involved in the post-transcriptional regulation of gene expression[1][2][3]. It contains a conserved PAT1 domain responsible for its mRNA-binding capabilities[1]. PATL2 is predominantly expressed in oocytes, with levels peaking in immature and growing oocytes and declining during oocyte maturation[3]. It acts as a translational repressor for maternal mRNAs, ensuring proper oocyte development and meiotic maturation[3]. Mutations in PATL2 have been linked to female infertility due to oocyte maturation arrest, affecting the MAPK pathway and Mos protein translation[3]. In addition to its cytoplasmic role in mRNA regulation and decay, PATL2 also facilitates the transcription of certain ion channels (like hERG/KCNH2 and KCNQ1) by interacting with components of the transcriptional machinery (e.g., TFIIE)[2]. PATL2 does not directly interact with ion channel proteins but regulates their biogenesis at the mRNA synthesis level[2]. It is essential for oocyte quality and fertility, with functional disruptions linked to reproductive disorders. No drugs currently target PATL2 directly.

Other names
PATL2Pat1ahPat1aPAT1-like protein 2Protein PAT1 homolog aprotein associated with topoisomerase II homolog 2OOMD4OZEMA4P100 (Xenopus)
02

Mechanism of action

Not applicable for drugs since PATL2 is not a direct drug target. Mechanistically, PATL2 acts by regulating mRNA transcription, decay, and translation of specific genes (including KCNH2/hERG and KCNQ1)[2].

03

Biological functions

Regulation of mRNA decayTranslational repression of maternal mRNAsFacilitation of transcription for specific potassium channels (e.g., hERG, KCNQ1)Oocyte maturation and meiosis regulation
04

Disease associations

Female infertility due to oocyte maturation arrestImpaired MAPK signaling pathway in oocytesPotential role in arrhythmia/cardiac channelopathies (via regulation of hERG/KCNQ1 transcription)
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Safety considerations

Overexpression or loss of PATL2 expression causes oocyte maturation arrest[1][3]Improper regulation may impair early embryonic development or gametogenesis
06

Biomarkers

Mutations in PATL2 (e.g., c.649T>A p.Tyr217Asn) are biomarkers for oocyte maturation arrest and primary infertility[3]

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