Two novel CAII mutations causing carbonic anhydrase II deficiency syndrome in two unrelated Chinese families

• Published in: Metabolic brain disease 2015-08, Vol.30 (4), p.989-997
• Main Authors: Pang, Qianqian, Qi, Xuan, Jiang, Yan, Wang, Ou, Li, Mei, Xing, Xiaoping, Dong, Jin, Xia, Weibo
• Format: Article
• Language: English
• Subjects: Acidosis, Renal Tubular - diagnosis; Acidosis, Renal Tubular - genetics; Adolescent; Asian Continental Ancestry Group - genetics; Biochemistry; Biomedical and Life Sciences; Biomedicine; Carbonic Anhydrase II - chemistry; Carbonic Anhydrase II - genetics; Carbonic Anhydrases - deficiency; Carbonic Anhydrases - genetics; Child, Preschool; Female; Humans; Male; Metabolic Diseases; Mutation - genetics; Neurology; Neurosciences; Oncology; Osteopetrosis - diagnosis; Osteopetrosis - genetics; Pedigree; Protein Structure, Secondary; Research Article; Urea Cycle Disorders, Inborn - diagnosis; Urea Cycle Disorders, Inborn - genetics
• ISSN: 0885-7490; 1573-7365
• DOI: 10.1007/s11011-015-9660-6

The carbonic anhydrase II (CAII) deficiency syndrome is a rare autosomal recessive osteopetrosis with renal tubular acidosis (RTA) and cerebral calcifications (MIM259730). CAII deficiency syndrome is caused by mutations in the gene CAII , which encodes the enzyme carbonic anhydrase II. CAII mutations are rarely reported in the Asian population. Here, we described two unrelated CAII deficiency families of Chinese Han origin with clinical and genetic analysis. Altogether, 106 subjects, including 2 probands, 4 unaffected family members from two non-consanguineous Chinese families, and 100 healthy controls were recruited. All seven exons and the exon-intron boundaries of the CAII gene were amplified and directly sequenced. Reverse transcription PCR (RT-PCR) was used to study the effect of splice site mutation. All clinical and biochemical parameters of the probands were collected. Two novel mutations of CAII gene were identified by mutational analysis: A nonsense mutation in exon 4 (c.T381C p.Y127X) in both families; a splice mutation at the splice donor site of intron 3 (c.350+2T>C, IVS3+2T>C) in one family. The splice-site mutation causes exon 3 skipping in patient’s mRNA resulting in an in-frame deletion and a novel premature stop codon. These mutations were predicted to result in a loss of function of CAII. This is the first report of CAII deficiency syndrome in Chinese population. Our findings extent the spectrum of CAII mutations observed in patients with CAII deficiency syndrome.