Analysis of RP2 and RPGR Mutations in Five X-Linked Chinese Families with Retinitis Pigmentosa

作者：Jiang, Jingjing; Wu, Xiaofei; Shen, Di; Dong, Lijin; Jiao, Xiaodong; Hejtmancik, J. Fielding^*; Li, Ningdong^*

来源：Scientific Reports, 2017, 7(1): 44465.

DOI：10.1038/srep44465

• NORTH-AMERICAN COHORT
• RETINITIS-PIGMENTOSA-2 PROTEIN
• COFACTOR-C
• GENE
• IDENTIFICATION
• LOCUS
• DYSTROPHY
• LINKAGE
• TRANSCRIPTION
• SPECTRUM

Mutations in RP2 and RPGR genes are responsible for the X-linked retinitis pigmentosa (XLRP). In this study, we analyzed the RP2 and RPGR gene mutations in five Han Chinese families with XLRP. An approximately 17Kb large deletion including the exon 4 and exon 5 of RP2 gene was found in an XLRP family. In addition, four frameshift mutations including three novel mutations of c. 1059 +1 G > T, c. 2002dupC and c. 2236_2237del CT, as well as a previously reported mutation of c. 2899delG were detected in the RPGR gene in the other four families. Our study further expands the mutation spectrum of RP2 and RPGR, and will be helpful for further study molecular pathogenesis of XLRP.

• 出版日期2017-3-15
• 单位首都医科大学; NIH; 天津医科大学