Novel compound heterozygous OBSCN variants in Chinese children with congenital pulmonary airway malformation
Jiali Xu, Siyu Ma, Zhaocong Yang, Yang Xu, Jirong Qi, Min Da, Xuming Mo

TL;DR
This study identifies mutations in the OBSCN gene in Chinese children with congenital pulmonary airway malformation, suggesting a potential role in the condition's development.
Contribution
The study reports novel compound heterozygous OBSCN variants in CPAM patients and explores the gene's role in lung development.
Findings
Compound heterozygous OBSCN mutations were identified in two CPAM patients.
OBSCN protein expression was reduced in CPAM lung tissue and during mouse lung development.
OBSCN appears to play a key role in the pseudoglandular stage of lung development.
Abstract
Congenital pulmonary airway malformation (CPAM) belongs to rare lung abnormalities which may result in poor lung development outcomes. However, the etiology of CPAM has not been well described. In this study, whole-exome sequencing (WES) technology was used to sequence 9 CPAM families to screen the pathogenic genes and their mutations for CPAM. Sanger sequencing was performed for verify the functions of these mutations. We found compound heterozygous mutations in OBSCN gene in two patients with CPAM: one with p.G8837A mutation inherited from her father and p.G1126S mutation inherited from her mother; the other with p.R5167W mutation inherited from his father and p.A7475T mutation inherited from his mother. Immunofluorescence results showed that the expression of OBSCN protein in the central lung tissue of CPAM patients was lower than that in the distal lung tissue of the lesion, and…
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Taxonomy
TopicsCongenital Diaphragmatic Hernia Studies · Tracheal and airway disorders · Neonatal Respiratory Health Research
