RESUMEN
BACKGROUND: Syndromic hearing loss that results from contiguous gene deletions is uncommon. Deafness-infertility syndrome (DIS) is caused by large contiguous gene deletions at 15q15.3. METHODS: Three families with a novel syndrome characterised by deafness and infertility are described. These three families do not share a common ancestor and do not share identical deletions. Linkage was established by completing a genome-wide scan and candidate genes in the linked region were screened by direct sequencing. RESULTS: The deleted region is about 100 kb long and involves four genes (KIAA0377, CKMT1B, STRC and CATSPER2), each of which has a telomeric duplicate. This genomic architecture underlies the mechanism by which these deletions occur. CATSPER2 and STRC are expressed in the sperm and inner ear, respectively, consistent with the phenotype in persons homozygous for this deletion. A deletion of this region has been reported in one other family segregating male infertility and sensorineural deafness, although congenital dyserythropoietic anaemia type I (CDAI) was also present, presumably due to a second deletion in another genomic region. CONCLUSION: We have identified three families segregating an autosomal recessive contiguous gene deletion syndrome characterised by deafness and sperm dysmotility. This new syndrome is caused by the deletion of contiguous genes at 15q15.3.
Asunto(s)
Cromosomas Humanos Par 15/genética , Eliminación de Gen , Pérdida Auditiva Sensorineural/genética , Infertilidad Masculina/genética , Secuencias Repetitivas de Ácidos Nucleicos , Secuencias Repetidas en Tándem , Secuencia de Bases , Canales de Calcio , Rotura Cromosómica , Mapeo Cromosómico , Cromosomas Humanos Par 15/ultraestructura , Consanguinidad , Creatina Quinasa/deficiencia , Creatina Quinasa/genética , Genes Recesivos , Haplotipos , Humanos , Péptidos y Proteínas de Señalización Intercelular , Canales Iónicos/deficiencia , Canales Iónicos/genética , Canales Iónicos/fisiología , Irán , Masculino , Proteínas de la Membrana/genética , Proteínas de la Membrana/fisiología , Datos de Secuencia Molecular , Conformación de Ácido Nucleico , Linaje , Fosfotransferasas (Aceptor del Grupo Fosfato) , Proteínas Tirosina Fosfatasas/genética , Seudogenes , Proteínas de Plasma Seminal , Alineación de Secuencia , Motilidad Espermática/genética , SíndromeRESUMEN
BACKGROUND: Larsen syndrome is an autosomal dominant osteochondrodysplasia characterised by large-joint dislocations and craniofacial anomalies. Recently, Larsen syndrome was shown to be caused by missense mutations or small inframe deletions in FLNB, encoding the cytoskeletal protein filamin B. To further delineate the molecular causes of Larsen syndrome, 20 probands with Larsen syndrome together with their affected relatives were evaluated for mutations in FLNB and their phenotypes studied. METHODS: Probands were screened for mutations in FLNB using a combination of denaturing high-performance liquid chromatography, direct sequencing and restriction endonuclease digestion. Clinical and radiographical features of the patients were evaluated. RESULTS AND DISCUSSION: The clinical signs most frequently associated with a FLNB mutation are the presence of supernumerary carpal and tarsal bones and short, broad, spatulate distal phalanges, particularly of the thumb. All individuals with Larsen syndrome-associated FLNB mutations are heterozygous for either missense or small inframe deletions. Three mutations are recurrent, with one mutation, 5071G-->A, observed in 6 of 20 subjects. The distribution of mutations within the FLNB gene is non-random, with clusters of mutations leading to substitutions in the actin-binding domain and filamin repeats 13-17 being the most common cause of Larsen syndrome. These findings collectively define autosomal dominant Larsen syndrome and demonstrate clustering of causative mutations in FLNB.
Asunto(s)
Anomalías Múltiples/genética , Proteínas Contráctiles/genética , Cifosis/genética , Proteínas de Microfilamentos/genética , Mutación , Columna Vertebral/anomalías , ADN/genética , ADN/aislamiento & purificación , Femenino , Filaminas , Falanges de los Dedos de la Mano/anomalías , Humanos , Masculino , Metacarpo/anomalías , FenotipoRESUMEN
Syndromic hearing loss that results from contiguous gene deletions is uncommon.Three families with a novel syndrome characterised by deafness and infertility are described. Linkage was established by completing a genome-wide scan and candidate genes in the linked region were screened by direct sequencing. The deleted region is about 100 kb long and involves four genes (KIAA0377, CKMT1B, STRC and CATSPER2), each of which has a telomeric duplicate. This genomic architecture underlies the mechanism by which these deletions occur. CATSPER2 and STRC are expressed in the sperm and inner ear, respectively, consistent with the phenotype in persons homozygous for this deletion. A deletion of this region has been reported in one other family segregating male infertility and sensorineural deafness. We have identified three families segregating an autosomal recessive contiguous gene deletion syndrome characterised by deafness and sperm dysmotility. This new syndrome is caused by the deletion of contiguous genes at 15q15.3.