Expression profiling of white sponge nevus by RNA sequencing revealed pathological pathways. Issue 1 (December 2015)

• Record Type: Journal Article
• Authors: Cai, Wenping; Jiang, Beizhan; Feng, Tienan; Xue, Jinfeng; Yang, Jianhua; Chen, Zhenghu; Liu, Junjun; Wei, Rongbin; Liu, Shangfeng; Zhao, Shouliang; Wang, Xiaoping
• Is Part Of: Orphanet journal of rare diseases. Volume 9:Issue 1(2014)
• Page Start: 1
• Page End: 10
• Publication Date: 2015-12
• Subjects: White sponge nevus -- Keratin7 -- Keratin13 -- Ubiquitin C (UBC) -- RNA sequencing (RNA-seq); Rare diseases -- Periodicals; Genetic disorders -- Periodicals; Orphan drugs -- Periodicals; 616
• DOI: 10.1186/s13023-015-0285-y
• Languages: English
• ISSNs: 1750-1172

Abstract

Abstract Background White sponge nevus (WSN) is a rare periodontal hereditary disease. To date, almost all WSN studies have focused on case reports or mutation reports. Thus, the mechanism behind WSN is still unclear. We investigated the pathogenesis of WSN using expression profiling. Methods Sequence analysis of samples from a WSN Chinese family revealed a mutation (332 T > C) in theKRT 13 gene that resulted in the amino acid change Leu111Pro. The pathological pathway behind the WSN expression profile was investigated by RNA sequencing (RNA-seq). Results Construction of a heatmap revealed 24 activated genes and 57 reduced genes in the WSN patients. The ribosome structure was damaged in the WSN patients. Moreover, the translation rate was limited in the WSN patients, whereas ubiquitin-mediated proteolysis was enhanced. Conclusions Our results suggest that the abnormal degradation of the KRT13 protein in WSN patients may be associated with keratin 7 (KRT7) and an abnormal ubiquitination process.