A presumed missense mutation of RPGR causes abnormal RNA splicing with exon skipping

• Published in: American journal of ophthalmology 2004-09, Vol.138 (3), p.504-505
• Main Authors: Demirci, F.Yesim K., Radak, Amy L., Rigatti, Brian W., Mah, Tammy S., Gorin, Michael B.
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Biological and medical sciences; Child; Exons - genetics; Eye Proteins - genetics; Female; Guanine Nucleotide Exchange Factors - genetics; Humans; Male; Medical sciences; Mutation, Missense; Ophthalmology; Polymorphism, Restriction Fragment Length; Retinitis Pigmentosa - genetics; Retinopathies; Reverse Transcriptase Polymerase Chain Reaction; RNA Splicing - genetics; Sequence Deletion
• ISSN: 0002-9394; 1879-1891
• DOI: 10.1016/j.ajo.2004.04.019

A patient with retinitis pigmentosa demonstrated a novel RPGR mutation (213G>A, last base of exon 2) predicted to cause a missense change (G52R) in the final protein. This study was performed to determine whether this mutation altered the effectiveness of the adjacent splice site. Observational case report. Total RNA was extracted from leukocytes of the proband and his carrier mother. Reverse transcription–polymerase chain reaction (RT-PCR) was performed by using the primers flanking exon 2 of RPGR transcript, followed by gel purification and direct sequencing. Sequencing revealed skipping of exon 2 in the mutated transcript, leading to in-frame deletion of 42 amino acids affecting the critical RCC1-like domain. The last base of exons is conserved as “G” in 80% of splicing consensus sequences, yet when changed, can completely disrupt constitutive splicing as in this patient. Our data confirm that the evaluation of the effects of some DNA sequence alterations at the RNA level might have important implications for appropriate genotype-phenotype correlations.