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dc.contributor.authorZamani, Ghazala Y
dc.contributor.authorKhan, Ranjha
dc.contributor.authorKarim, Noreen
dc.contributor.authorAhmed, Zubair M
dc.contributor.authorNaeem, Muhammad
dc.date.accessioned2022-03-28T13:10:16Z
dc.date.available2022-03-28T13:10:16Z
dc.date.issued2022-03-19
dc.identifier.urihttp://hdl.handle.net/10713/18378
dc.description.abstractXeroderma pigmentosum (XP) is a rare autosomal recessive genetic disorder characterized by severe sensitivity of skin to sunlight and an increased risk of skin cancer. XP variant (XPV), a milder subtype, is caused by variants in the POLH gene. POLH encodes an error-prone DNA-polymerase eta (pol eta) which performs translesion synthesis past ultraviolet photoproducts. The current study documents the clinical and genetic investigations of two large consanguineous Pakistani families affected with XPV. In family 1, whole exome sequencing (WES) revealed a novel frameshift variant, c.1723dupG (p.(Val575Glyfs*4)), of POLH, which is predicted to cause frameshift and premature truncation of the encoded enzyme. Indeed, our ex vivo studies in HEK293T cells confirmed the truncation of the encoded protein due to the c.1723dupG variant. In family 2, Sanger sequencing of POLH exons, revealed a recurrent nonsense variant, c.437dupA (p.Tyr146*). POLH forms a hetero-tetrameric POLZ complex with REV3L, REV7, POLD2 and POLD3. Next, we performed in silico analysis of POLH and other POLZ complex genes expression in publicly available single cell mRNAseq datasets from adult human healthy and aging skin. We found overlapping expression of POLH, REV3L and POLD2 in multiple cell types including differentiated and undifferentiated keratinocytes, pericytes and melanocytes in healthy skin. However, in aging human skin, POLH expression is reduced in compare to its POLZ complex partners. Insights from our study will facilitate counseling regarding the molecular and phenotypic landscape of POLH-related XPV.en_US
dc.description.urihttps://doi.org/10.3390/genes13030543en_US
dc.language.isoenen_US
dc.publisherMDPI AGen_US
dc.relation.ispartofGenesen_US
dc.subjectPOLD2en_US
dc.subjectPOLHen_US
dc.subjectREV3Len_US
dc.subjectREV7en_US
dc.subjectautosomal recessiveen_US
dc.subjectpolymerase etaen_US
dc.subjectxeroderma pigmentosumen_US
dc.titleIdentification of Frameshift Variants in Gene Causing Xeroderma Pigmentosum in Two Consanguineous Pakistani Families.en_US
dc.typeArticleen_US
dc.identifier.doi10.3390/genes13030543
dc.identifier.pmid35328096
dc.source.journaltitleGenes
dc.source.volume13
dc.source.issue3
dc.source.countryUnited States
dc.source.countrySwitzerland


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