Identification of a Missense Mutation in the Surfactant Protein A2 Gene in a Chinese Family with Interstitial Lung Disease.

Abstract

Interstitial lung disease (ILD) is a large group of disorders, most of which lead to progressive scarring of lung tissue. The scarring associated with ILD eventually affects your ability to breathe and get enough oxygen into your bloodstream. The typical symptoms of ILD are shortness of breath at rest or aggravated by exertion and dry cough. In this study, we enrolled a family with ILDs from central south region of China. Three patients suffered from repeated cough and shortness of breath. The high resolution computed tomography (HRCT) testing further confirmed the diagnosis of interstitial lung lesions. Whole exome sequencing (WES) and Sanger sequencing were applied to detect the genetic lesion of the family. By employing WES, a novel heterozygous mutation (NM_001098668: c.554C>T/p.A185V) of surfactant protein A2 (SFTPA2) was identified in the affected individuals and absent in the healthy members. Bioinformatics analysis predicted that this mutation is disease-causing mutation and located in an evolutionarily conserved site of SFTPA2 protein. The novel mutation may disrupt the stability of SFTPA2 protein and induce endoplasmic reticulum stress, finally leading to ILD under the influence of microorganisms. Our study not only expands the spectrum of SFTPA2 mutations but also helps the family members to mitigate ILD risk factors. The study also supplements and improves genetic testing strategies and ILD risk estimation methodologies for China.

• Authors: Lv Liu, Yi-Jie Liu, Ting Guo, Hong Luo
• Journal: DNA and cell biology (DNA Cell Biol) Vol. 40 Issue 1 Pg. 126-131 (Jan 2021) ISSN: 1557-7430 [Electronic] United States
• PMID: 33181027 (Publication Type: Case Reports, Journal Article)

Chemical References

• Pulmonary Surfactant-Associated Protein A
• SFTPA2 protein, human

Topics

• Aged
• Female
• Humans
• Lung Diseases, Interstitial (genetics, pathology)
• Male
• Middle Aged
• Mutation, Missense
• Pedigree
• Protein Domains
• Protein Stability
• Pulmonary Surfactant-Associated Protein A (chemistry, genetics)