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HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder.

Authors :
Niggl E
Bouman A
Briere LC
Hoogenboezem RM
Wallaard I
Park J
Admard J
Wilke M
Harris-Mostert EDRO
Elgersma M
Bain J
Balasubramanian M
Banka S
Benke PJ
Bertrand M
Blesson AE
Clayton-Smith J
Ellingford JM
Gillentine MA
Goodloe DH
Haack TB
Jain M
Krantz I
Luu SM
McPheron M
Muss CL
Raible SE
Robin NH
Spiller M
Starling S
Sweetser DA
Thiffault I
Vetrini F
Witt D
Woods E
Zhou D
Elgersma Y
van Esbroeck ACM
Source :
American journal of human genetics [Am J Hum Genet] 2023 Aug 03; Vol. 110 (8), pp. 1414-1435.
Publication Year :
2023

Abstract

Heterogeneous nuclear ribonucleoprotein C (HNRNPC) is an essential, ubiquitously abundant protein involved in mRNA processing. Genetic variants in other members of the HNRNP family have been associated with neurodevelopmental disorders. Here, we describe 13 individuals with global developmental delay, intellectual disability, behavioral abnormalities, and subtle facial dysmorphology with heterozygous HNRNPC germline variants. Five of them bear an identical in-frame deletion of nine amino acids in the extreme C terminus. To study the effect of this recurrent variant as well as HNRNPC haploinsufficiency, we used induced pluripotent stem cells (iPSCs) and fibroblasts obtained from affected individuals. While protein localization and oligomerization were unaffected by the recurrent C-terminal deletion variant, total HNRNPC levels were decreased. Previously, reduced HNRNPC levels have been associated with changes in alternative splicing. Therefore, we performed a meta-analysis on published RNA-seq datasets of three different cell lines to identify a ubiquitous HNRNPC-dependent signature of alternative spliced exons. The identified signature was not only confirmed in fibroblasts obtained from an affected individual but also showed a significant enrichment for genes associated with intellectual disability. Hence, we assessed the effect of decreased and increased levels of HNRNPC on neuronal arborization and neuronal migration and found that either condition affects neuronal function. Taken together, our data indicate that HNRNPC haploinsufficiency affects alternative splicing of multiple intellectual disability-associated genes and that the developing brain is sensitive to aberrant levels of HNRNPC. Hence, our data strongly support the inclusion of HNRNPC to the family of HNRNP-related neurodevelopmental disorders.<br />Competing Interests: Declaration of interests The authors declare no competing interests.<br /> (Copyright © 2023 American Society of Human Genetics. All rights reserved.)

Details

Language :
English
ISSN :
1537-6605
Volume :
110
Issue :
8
Database :
MEDLINE
Journal :
American journal of human genetics
Publication Type :
Academic Journal
Accession number :
37541189
Full Text :
https://doi.org/10.1016/j.ajhg.2023.07.005