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Role of BRCA1-associated protein (BRAP) variant in childhood pulmonary arterial hypertension

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Chida-Nagai, Ayako 
Shintani, Masaki 
Sato, Hiroki 
Nakayama, Tomotaka 
Nii, Masaki 


Although mutations in several genes have been reported in pulmonary arterial hypertension (PAH), most of PAH cases do not carry these mutations. This study aimed to identify a novel cause of PAH. To determine the disease-causing variants, direct sequencing and multiplex ligation-dependent probe amplification were performed to analyze 18 families with multiple affected family members with PAH. In one of the 18 families with PAH, no disease-causing variants were found in any of BMPR2, ACVRL1, ENG, SMAD1/4/8, BMPR1B, NOTCH3, CAV1, or KCNK3. In this family, a female proband and her paternal aunt developed PAH in their childhood. Whole-exome next-generation sequencing was performed in the 2 PAH patients and the proband’s healthy mother, and a BRCA1-associated protein (BRAP) gene variant, p.Arg554Leu, was identified in the 2 family members with PAH, but not in the proband’s mother without PAH. Functional analyses were performed using human pulmonary arterial smooth muscle cells (hPASMCs). Knockdown of BRAP via small interfering RNA in hPASMCs induced p53 signaling pathway activation and decreased cell proliferation. Overexpression of either wild-type BRAP or p.Arg554Leu-BRAP cDNA constructs caused cell death confounding these studies, however we observed higher levels of p53 signaling inactivation and hPASMC proliferation in cells expressing p.Arg554Leu-BRAP compared to wild-type BRAP. In addition, p.Arg554Leu-BRAP induced decreased apoptosis of hPASMCs compared with wild-type BRAP. In conclusion, we have identified a novel variant of BRAP in a Japanese family with PAH and our results suggest it could have a gain-of-function. This study sheds light on new mechanism of PAH pathogenesis.



Adolescent, Adult, Apoptosis, Cells, Cultured, Child, Child, Preschool, Exome, Familial Primary Pulmonary Hypertension, Female, Humans, Infant, Male, Muscle, Smooth, Vascular, Mutation, Pedigree, Pulmonary Artery, Signal Transduction, Ubiquitin-Protein Ligases, Exome Sequencing, Young Adult

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Public Library of Science (PLoS)
his work was supported by MEXT KAKENHI Grant Number 15K19639 (