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来自蒙古的两个母系遗传氨基糖苷类耳毒性家族的线粒体12S rRNA基因突变。

Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.

作者信息

Pandya A, Xia X, Radnaabazar J, Batsuuri J, Dangaansuren B, Fischel-Ghodsian N, Nance W E

机构信息

Department of Human Genetics, Medical College of Virginia, Richmond 23298, USA.

出版信息

J Med Genet. 1997 Feb;34(2):169-72. doi: 10.1136/jmg.34.2.169.

Abstract

Irreversible hearing loss is a catastrophic complication of treatment with aminoglycoside antibiotics such as streptomycin, gentamycin, and kanamycin. Many kindreds showing a matrilineal pattern of inheritance of this trait have been described in China where the widespread use of aminoglycoside antibiotics accounts for approximately 25% of profound deafness in some districts. Because of the characteristic inheritance pattern, mitochondrial DNA (mtDNA) mutations were postulated to be the cause of the deafness in these pedigrees. In 1993 it was shown that an A to G substitution at base pair 1555 of the mitochondrial 12S ribosomal RNA gene was the only mutation common to all the families with aminoglycoside ototoxicity. We ascertained three Mongolian pedigrees from the School for the Deaf and Blind in Ulaanbaatar, all of which contained multiple affected subjects with streptomycin induced deafness in a pattern consistent with matrilineal transmission. Amplified mtDNA, obtained from transformed lymphoblastoid cell lines using previously described primers, showed the A to G point mutation in the 12S rRNA gene in two of the three families by restriction analysis as well as direct sequencing. No other example of this substitution was found among 400 control samples from Mongolians with normal hearing. We have thus confirmed the clinical relevance of the 1555 A to G mitochondrial mutation in the 12S rRNA gene by identifying it in affected subjects with familial aminoglycoside ototoxicity in another ethnic group. In countries where aminoglycosides are widely used, genetic counselling and screening of high risk families before the use of these drugs could have a dramatic effect on the incidence of deafness.

摘要

不可逆性听力丧失是链霉素、庆大霉素和卡那霉素等氨基糖苷类抗生素治疗的灾难性并发症。在中国,许多呈现这种性状母系遗传模式的家族被报道,在一些地区,氨基糖苷类抗生素的广泛使用约占重度耳聋病例的25%。由于其独特的遗传模式,线粒体DNA(mtDNA)突变被推测为这些家系中耳聋的病因。1993年,研究表明线粒体12S核糖体RNA基因第1555位碱基对由A到G的替换是所有氨基糖苷类耳毒性家族共有的唯一突变。我们从乌兰巴托的聋哑学校确定了三个蒙古族家系,所有家系都有多名受影响个体,呈现出与母系遗传一致的链霉素诱导性耳聋模式。使用先前描述的引物从转化的淋巴母细胞系中获得的扩增mtDNA,通过限制性分析和直接测序显示,三个家系中的两个家系12S rRNA基因存在A到G的点突变。在400名听力正常的蒙古族对照样本中未发现该替换的其他例子。因此,我们通过在另一个种族的家族性氨基糖苷类耳毒性受影响个体中鉴定出12S rRNA基因中1555 A到G的线粒体突变,证实了该突变的临床相关性。在氨基糖苷类广泛使用的国家,在使用这些药物之前对高危家族进行遗传咨询和筛查可能会对耳聋发病率产生显著影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17f2/1050876/a5ad785970a1/jmedgene00244-0082-a.jpg

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