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A biallelic frameshift indel in PPP1R35 as a cause of primary microcephaly.

Authors :
Dawood, Moez
Akay, Gulsen
Mitani, Tadahiro
Marafi, Dana
Fatih, Jawid M.
Gezdirici, Alper
Najmabadi, Hossein
Kahrizi, Kimia
Punetha, Jaya
Grochowski, Christopher M.
Du, Haowei
Jolly, Angad
Li, He
Coban‐Akdemir, Zeynep
Sedlazeck, Fritz J.
Hunter, Jill V.
Jhangiani, Shalini N.
Muzny, Donna
Pehlivan, Davut
Posey, Jennifer E.
Source :
American Journal of Medical Genetics. Part A; Mar2023, Vol. 191 Issue 3, p794-804, 11p
Publication Year :
2023

Abstract

Protein phosphatase 1 regulatory subunit 35 (PPP1R35) encodes a centrosomal protein required for recruiting microtubule‐binding elongation machinery. Several proteins in this centriole biogenesis pathway correspond to established primary microcephaly (MCPH) genes, and multiple model organism studies hypothesize PPP1R35 as a candidate MCPH gene. Here, using exome sequencing (ES) and family‐based rare variant analyses, we report a homozygous, frameshifting indel deleting the canonical stop codon in the last exon of PPP1R35 [Chr7: c.753_*3delGGAAGCGTAGACCinsCG (p.Trp251Cysfs*22)]; the variant allele maps in a 3.7 Mb block of absence of heterozygosity (AOH) in a proband with severe MCPH (−4.3 SD at birth, −6.1 SD by 42 months), pachygyria, and global developmental delay from a consanguineous Turkish kindred. Droplet digital PCR (ddPCR) confirmed mutant mRNA expression in fibroblasts. In silico prediction of the translation of mutant PPP1R35 is expected to be elongated by 18 amino acids before encountering a downstream stop codon. This complex indel allele is absent in public databases (ClinVar, gnomAD, ARIC, 1000 genomes) and our in‐house database of 14,000+ exomes including 1800+ Turkish exomes supporting predicted pathogenicity. Comprehensive literature searches for PPP1R35 variants yielded two probands affected with severe microcephaly (−15 SD and −12 SD) with the same homozygous indel from a single, consanguineous, Iranian family from a cohort of 404 predominantly Iranian families. The lack of heterozygous cases in two large cohorts representative of the genetic background of these two families decreased our suspicion of a founder allele and supports the contention of a recurrent mutation. We propose two potential secondary structure mutagenesis models for the origin of this variant allele mediated by hairpin formation between complementary GC rich segments flanking the stop codon via secondary structure mutagenesis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15524825
Volume :
191
Issue :
3
Database :
Complementary Index
Journal :
American Journal of Medical Genetics. Part A
Publication Type :
Academic Journal
Accession number :
161862831
Full Text :
https://doi.org/10.1002/ajmg.a.63080