1. An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis
- Author
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Shogo Minamikawa, Takeshi Ninchoji, Ichiro Morioka, Nobuo Mori, Koichi Nakanishi, Keita Nakanishi, Hiroshi Kaito, Yuya Miyoshi, Taniguchi Ikeda Mariko, Rika Fujimaru, Kazumoto Iijima, Masafumi Matsuo, Tomohiko Yamamura, Junya Fujimura, Kandai Nozu, and Tomoko Horinouchi
- Subjects
Male ,0301 basic medicine ,Vacuolar Proton-Translocating ATPases ,medicine.medical_specialty ,ATP6V0A4 ,lcsh:RC870-923 ,medicine.disease_cause ,Compound heterozygosity ,03 medical and health sciences ,Exon ,Minigene ,Internal medicine ,medicine ,Consensus sequence ,Humans ,Protein Splicing ,Gene ,Autosomal recessive distal renal tubular acidosis ,Genetics ,Mutation ,Base Sequence ,business.industry ,Intron ,Genetic Variation ,Infant ,Acidosis, Renal Tubular ,lcsh:Diseases of the genitourinary system. Urology ,Introns ,030104 developmental biology ,Splicing assay ,Nephrology ,RNA splicing ,business ,Research Article - Abstract
Background: Autosomal recessive distal renal tubular acidosis (dRTA) is a rare hereditary disease caused by pathogenic variants in the ATP6V0A4 gene or ATP6V1B1 gene, and characterized by hyperchloremic metabolic acidosis with normal anion gap, hypokalemia, hypercalciuria, hypocitraturia and nephrocalcinosis. Although several intronic nucleotide variants in these genes have been detected, all of them fell in the apparent splice consensus sequence. In general, transcriptional analysis is necessary to determine the effect on function of the novel intronic variants located out of splicing consensus sequences. In recent years, functional splicing analysis using minigene construction was used to assess the pathogenicity of novel intoronic variant in various field. Methods: We investigated a sporadic case of dRTA with a compound heterozygous mutation in the ATP6V0A4 gene, revealed by next generation sequencing. One variant was already reported as pathogenic; however, the other was a novel variant in intron 11 (c. 1029 + 5G > A) falling outside of the apparent splicing consensus sequence. Expression of ATP6V0A4 was not detected in peripheral leukocytes by RT-PCR analysis. Therefore, an in vitro functional splicing study using minigene construction was conducted to analyze the splicing pattern of the novel variant. Results: A minigene assay revealed that the novel intronic variant leads to a 104 bp insertion immediately following exon 11. In addition, this result was confirmed using RNA extracted from the patient's cultured leukocytes. Conclusion: These results proved the pathogenicity of a novel intronic variant in our patient. We concluded that the minigene assay is a useful, non-invasive method for functional splicing analysis of inherited kidney disease, even if standard transcriptional analysis could not detect abnormal mRNA., 論文
- Published
- 2017
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