RESUMEN
The homeodomain transcription factor SHOX2 is involved in the development and function of the heart's primary pacemaker, the sinoatrial node (SAN), and has been associated with cardiac conduction-related diseases such as atrial fibrillation and sinus node dysfunction. To shed light on Shox2-dependent genetic processes involved in these diseases, we established a murine embryonic stem cell (ESC) cardiac differentiation model to investigate Shox2 pathways in SAN-like cardiomyocytes. Differential RNA-seq-based expression profiling of Shox2+/+ and Shox2-/- ESCs revealed 94 dysregulated transcripts in Shox2-/- ESC-derived SAN-like cells. Of these, 15 putative Shox2 target genes were selected for further validation based on comparative expression analysis with SAN- and right atria-enriched genes. Network-based analyses, integrating data from the Mouse Organogenesis Cell Atlas and the Ingenuity pathways, as well as validation in mouse and zebrafish models confirmed a regulatory role for the novel identified Shox2 target genes including Cav1, Fkbp10, Igfbp5, Mcf2l and Nr2f2. Our results indicate that genetic networks involving SHOX2 may contribute to conduction traits through the regulation of these genes.
Asunto(s)
Relojes Biológicos/fisiología , Proteínas de Homeodominio/metabolismo , Células Madre Embrionarias de Ratones/metabolismo , Miocitos Cardíacos/metabolismo , Organogénesis/fisiología , Nodo Sinoatrial/embriología , Factores de Transcripción/metabolismo , Proteínas de Pez Cebra/metabolismo , Pez Cebra/embriología , Animales , Diferenciación Celular , Proteínas de Homeodominio/genética , Humanos , Ratones , Ratones Noqueados , Células Madre Embrionarias de Ratones/citología , Miocitos Cardíacos/citología , Nodo Sinoatrial/citología , Factores de Transcripción/genética , Pez Cebra/genética , Proteínas de Pez Cebra/genéticaRESUMEN
Recent genetic data on schizophrenia (SCZ) have suggested that proteins of the postsynaptic density of excitatory synapses have a role in its etiology. Mutations in the three SHANK genes encoding for postsynaptic scaffolding proteins have been shown to represent risk factors for autism spectrum disorders and other neurodevelopmental disorders. To address if SHANK2 variants are associated with SCZ, we sequenced SHANK2 in 481 patients and 659 unaffected individuals. We identified a significant increase in the number of rare (minor allele frequency<1%) SHANK2 missense variants in SCZ individuals (6.9%) compared with controls (3.9%, P=0.039). Four out of fifteen non-synonymous variants identified in the SCZ cohort (S610Y, R958S, P1119T and A1731S) were selected for functional analysis. Overexpression and knockdown-rescue experiments were carried out in cultured primary hippocampal neurons with a major focus on the analysis of morphological changes. Furthermore, the effect on actin polymerization in fibroblast cell lines was investigated. All four variants revealed functional impairment to various degrees, as a consequence of alterations in spine volume and clustering at synapses and an overall loss of presynaptic contacts. The A1731S variant was identified in four unrelated SCZ patients (0.83%) but not in any of the sequenced controls and public databases (P=4.6 × 10(-5)). Patients with the A1731S variant share an early prodromal phase with an insidious onset of psychiatric symptoms. A1731S overexpression strongly decreased the SHANK2-Bassoon-positive synapse number and diminished the F/G-actin ratio. Our results strongly suggest a causative role of rare SHANK2 variants in SCZ and underline the contribution of SHANK2 gene mutations in a variety of neuropsychiatric disorders.
Asunto(s)
Proteínas del Tejido Nervioso/genética , Esquizofrenia/genética , Adulto , Animales , Células COS , Chlorocebus aethiops , Estudios de Cohortes , Análisis Mutacional de ADN , Femenino , Técnicas de Silenciamiento del Gen , Células HEK293 , Hipocampo/citología , Hipocampo/metabolismo , Humanos , Masculino , Mutación , Proteínas del Tejido Nervioso/metabolismo , Neuronas/metabolismo , Estructura Terciaria de Proteína , Ratas , Ratas Sprague-Dawley , Esquizofrenia/metabolismoRESUMEN
Neurodevelopmental disorders are multi-faceted and can lead to intellectual disability, autism spectrum disorder and language impairment. Mutations in the Forkhead box FOXP1 gene have been linked to all these disorders, suggesting that it may play a central role in various cognitive and social processes. To understand the role of Foxp1 in the context of neurodevelopment leading to alterations in cognition and behaviour, we generated mice with a brain-specific Foxp1 deletion (Nestin-Cre(Foxp1-/-)mice). The mutant mice were viable and allowed for the first time the analysis of pre- and postnatal neurodevelopmental phenotypes, which included a pronounced disruption of the developing striatum and more subtle alterations in the hippocampus. More detailed analysis in the CA1 region revealed abnormal neuronal morphogenesis that was associated with reduced excitability and an imbalance of excitatory to inhibitory input in CA1 hippocampal neurons in Nestin-Cre(Foxp1-/-) mice. Foxp1 ablation was also associated with various cognitive and social deficits, providing new insights into its behavioural importance.
Asunto(s)
Trastorno Autístico/genética , Discapacidades del Desarrollo/genética , Factores de Transcripción Forkhead/deficiencia , Proteínas Represoras/deficiencia , Estimulación Acústica , Animales , Animales Recién Nacidos , Encéfalo/crecimiento & desarrollo , Encéfalo/patología , Proliferación Celular/genética , Dendritas/patología , Discapacidades del Desarrollo/patología , Factores de Transcripción Forkhead/genética , Hipocampo/patología , Técnicas In Vitro , Masculino , Trastornos de la Memoria/genética , Memoria a Corto Plazo/fisiología , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Neuronas/patología , Neuronas/fisiología , Inhibición Prepulso/genética , Proteínas Represoras/genética , Trastorno de la Conducta Social/genética , Transmisión Sináptica/genéticaRESUMEN
The homeobox gene SHOX encodes a transcription factor which is important for normal limb development. Approximately 5 to 10% of short patients exhibit a mutation or deletion in either the SHOX gene or its downstream enhancer regions. In humans, SHOX deficiency has been associated with various short stature syndromes as well as non-syndromic idiopathic short stature. A common feature of these syndromes is disproportionate short stature with a particular shortening of the forearms and lower legs. Madelung deformity, cubitus valgus, high-arched palate and muscular hypertrophy also differed markedly between patients with or without SHOX gene defects. A clinical trial in patients with SHOX deficiency and Turner syndrome demonstrated highly significant growth hormone-stimulated increases in height velocity and height SDS in both groups. Employing microarray analyses and cell culture experiments, a strong effect of SHOX on the expression of the natriuretic peptide BNP and the fibroblast growth factor receptor gene FGFR3 could be demonstrated. We found that BNP was positively regulated, while Fgfr3 was negatively regulated by SHOX. A regulation that occurs mainly in the mesomelic segments, a region where SHOX is known to be strongly expressed, offers a possible explanation for the phenotypes seen in patients with FGFR3 (e.g. achondroplasia) and SHOX defects (e.g. Léri-Weill dyschondrosteosis).
Asunto(s)
Estatura/genética , Regulación de la Expresión Génica , Trastornos del Crecimiento/genética , Proteínas de Homeodominio/genética , Síndrome de Turner/genética , Proteínas de Homeodominio/metabolismo , Humanos , Mutación , Proteína de la Caja Homeótica de Baja EstaturaRESUMEN
Microdeletions including 5q31 have been reported in only few patients to date. Apart from intellectual disability/developmental delay (ID/DD) of varying degrees, which is common to all reported patients, the clinical spectrum is wide and includes short stature, failure to thrive, congenital heart defects, encephalopathies, and dysmorphic features. We report a patient with a 0.9-Mb de novo deletion in 5q31.2, the smallest microdeletion in 5q31 reported thus far. His clinical presentation includes mild DD, borderline short stature, postnatal microcephaly, and mild dysmorphic signs including microretrognathia. Together with data from 7 reported overlapping microdeletions, analysis of our patient enabled the tentative delineation of a phenotype map for 5q31 deletions. In contrast to the mild phenotype of small microdeletions affecting only 5q31.2, carriers of larger microdeletions which also include subbands 5q31.1 and/or 5q31.3 seem to be more severely affected with congenital malformations, growth anomalies, and severe encephalopathies. A 240-kb smallest region of overlap in 5q31.2 is delineated which contains only 2 genes, CTNNA1 and LRRTM2. We propose LRRTM2 as the most promising candidate gene for ID/DD due to its expression pattern, function as a key regulator of excitatory development, and interaction with Neurexin 1. However, sequence analysis of LRRTM2 in 330 patients with ID/DD revealed no relevant alterations, excluding point mutations in LRRTM2 as a frequent cause of ID/DD in patients without microdeletions.
RESUMEN
Mesenchymal stem cells (MSCs) are multipotent cells capable of differentiation into several mesodermal lineages. These cells have been isolated from various tissues, such as adult bone marrow, placenta, and fetal tissues. The comparative potential of these cells originating from different tissues to differentiate into the chondrogenic lineage is still not fully defined. The aim of our study was to investigate the chondrogenic potential of MSCs isolated from different sources. MSCs from fetal and adult tissues were phenotypically characterized and examined for their differentiation capacity, based on morphological criteria and expression of extracellular matrix components. Our results show that both fetal and adult MSCs have chondrogenic potential under appropriate conditions. The capacity of bone marrow-derived MSCs to differentiate into chondrocytes was reduced on passaging of cells. MSCs of bone marrow origin, either fetal or adult, exhibit a better chondrogenesis than fetal lung- and placenta-derived MSCs, as demonstrated by the appearance of typical morphological features of cartilage, the intensity of toluidine blue staining, and the expression of collagen type II, IX, and X after culture under chondrogenic conditions. As MSCs represent an attractive tool for cartilage tissue repair strategies, our data suggest that bone marrow should be considered the preferred MSC source for these therapeutic approaches.
Asunto(s)
Células de la Médula Ósea/citología , Diferenciación Celular , Condrogénesis , Células Madre Mesenquimatosas/citología , Adipogénesis , Proliferación Celular , Forma de la Célula , Células Cultivadas , Femenino , Humanos , Inmunofenotipificación , OsteogénesisRESUMEN
Comparative FISH mapping of PAC clones covering almost 3 Mb of the human AZFa region in Yq11.21 to metaphases of human and great apes unravels breakpoints that were involved in species-specific Y chromosome evolution. An astonishing clustering of evolutionary breakpoints was detected in the very proximal region on the long arm of the human Y chromosome in Yq11.21. These breakpoints were involved in deletions, one specific for the human and another for the orang-utan Y chromosome, in a duplicative translocation/transposition specific for bonobo and chimpanzee Y chromosomes and in a pericentric inversion specific for the gorilla Y chromosome. In addition, our comparative results allow the deduction of a model for the human Y chromosome evolution.
Asunto(s)
Rotura Cromosómica/genética , Cromosomas Humanos Y/genética , Evolución Molecular , Primates/genética , Cromosoma Y/genética , Animales , Mapeo Cromosómico/métodos , Cromosomas Artificiales de Bacteriófagos P1/genética , Cromosomas Humanos X/genética , Cromosomas de los Mamíferos/genética , Gorilla gorilla/genética , Humanos , Hibridación Fluorescente in Situ/métodos , Linfocitos/química , Linfocitos/citología , Linfocitos/metabolismo , Macaca nemestrina/genética , Masculino , Metafase/genética , Pan troglodytes/genética , Pongo pygmaeus/genética , Cromosoma X/genéticaRESUMEN
Clones of a PAC contig encompassing the human AZFa region in Yq11.21 were comparatively FISH mapped to great ape Y chromosomes. While the orthologous AZFa locus in the chimpanzee, the bonobo and the gorilla maps to the long arm of their Y chromosomes in Yq12.1-->q12.2, Yq13.1-->q13.2 and Yq11.2, respectively, it is found on the short arm of the orang-utan subspecies of Borneo and Sumatra, in Yp12.3 and Yp13.2, respectively. Regarding the order of PAC clones and genes within the AZFa region, no differences could be detected between apes and man, indicating a strong evolutionary stability of this non-recombining region.
Asunto(s)
Evolución Molecular , Primates/genética , Proteínas de Plasma Seminal/genética , Animales , Línea Celular , Cromosomas Artificiales de Bacteriófagos P1/genética , Cromosomas Humanos X/genética , Cromosomas Humanos Y/genética , Cromosomas de los Mamíferos/genética , Mapeo Contig/métodos , Sitios Genéticos , Gorilla gorilla/genética , Humanos , Hibridación Fluorescente in Situ/métodos , Linfocitos/química , Linfocitos/citología , Linfocitos/metabolismo , Macaca nemestrina/genética , Masculino , Pan troglodytes/genética , Pongo pygmaeus/genética , Cromosoma X/genética , Cromosoma Y/genéticaRESUMEN
Leri-Weill syndrome (LWS) is a skeletal dysplasia with mesomelic short stature, bilateral Madelung deformity (BMD) and SHOX (short stature homeobox-containing gene) haploinsufficiency. The effect of 24 months of recombinant human growth hormone (rhGH) therapy on the stature and BMD of two females with SHOX haploinsufficiency (demonstrated by fluorescence in situ hybridisation) and LWS was evaluated. Both patients demonstrated an increase in height standard deviation score (SDS) and height velocity SDS over the 24 months of therapy. Patient 1 demonstrated a relative increase in arm-span and upper segment measurements with rhGH while patient 2 demonstrated a relative increase in lower limb length. There was appropriate advancement of bone age, no adverse events and no significant deterioration in BMD. In this study, 24 months of rhGH was a safe and effective therapy for the disproportionate short stature of SHOX haploinsufficiency, with no clinical deterioration of BMD.
Asunto(s)
Estatura/efectos de los fármacos , Estatura/genética , Trastornos del Crecimiento/tratamiento farmacológico , Trastornos del Crecimiento/genética , Hormona del Crecimiento/uso terapéutico , Proteínas de Homeodominio/genética , Adolescente , Brazo/anatomía & histología , Brazo/crecimiento & desarrollo , Huesos/diagnóstico por imagen , Niño , Femenino , Mano/diagnóstico por imagen , Haplotipos , Humanos , Hibridación Fluorescente in Situ , Cariotipificación , Pierna/anatomía & histología , Pierna/crecimiento & desarrollo , Masculino , Fenotipo , Radiografía , Proteína de la Caja Homeótica de Baja EstaturaRESUMEN
This study was designed to determine the intrafamilial effect of SHOX haploinsufficiency on stature, by comparing the growth and phenotype of 26 SHOX haploinsufficient individuals with 45 relatives and population standards. It confirmed that SHOX haploinsufficiency leads to growth restriction from birth to final height. Compared to unaffected siblings, the SHOX haploinsufficient cohort was 2.14 SDS (3.8 cm) shorter at birth and 2.1 SDS shorter through childhood. At final height females were 2.4 SDS (14.4 cm) shorter and males 0.8 SDS (5.3 cm) shorter than normal siblings. The family height analysis suggests that the effect of SHOX haploinsufficiency on growth may have been previously underestimated at birth and overestimated in males at final height. SHOX haploinsufficiency leads to short arms in 92%, bilateral Madelung deformity in 73% and short stature in 54%. Females were more severely affected than males. We conclude that SHOX is a major growth gene and that mutations are associated with a broad range of phenotype.
Asunto(s)
Desarrollo Óseo/genética , Trastornos del Crecimiento/genética , Crecimiento/genética , Proteínas de Homeodominio/genética , Adolescente , Adulto , Determinación de la Edad por el Esqueleto , Anciano , Brazo/anatomía & histología , Brazo/crecimiento & desarrollo , Estatura/genética , Estatura/fisiología , Densidad Ósea/genética , Densidad Ósea/fisiología , Huesos/diagnóstico por imagen , Niño , Estudios de Cohortes , Femenino , Genotipo , Haplotipos , Humanos , Recién Nacido , Pierna/anatomía & histología , Pierna/crecimiento & desarrollo , Masculino , Persona de Mediana Edad , Linaje , Fenotipo , Proteína de la Caja Homeótica de Baja Estatura , SíndromeAsunto(s)
Estatura/genética , Genes Homeobox/genética , Proteínas de Homeodominio/genética , Mutación/genética , Osteocondrodisplasias/genética , Estudios de Cohortes , Femenino , Trastornos del Crecimiento/epidemiología , Trastornos del Crecimiento/genética , Humanos , Masculino , Osteocondrodisplasias/epidemiología , Linaje , Prevalencia , Proteína de la Caja Homeótica de Baja Estatura , SíndromeAsunto(s)
Estatura/genética , Centrómero/genética , Mapeo Cromosómico/métodos , Cromosoma Y/genética , Adulto , Deleción Cromosómica , Cromosomas Artificiales Bacterianos/genética , Cromosomas Artificiales de Bacteriófagos P1/genética , Femenino , Marcadores Genéticos/genética , Genotipo , Humanos , Hibridación Fluorescente in Situ/métodos , Masculino , Núcleo FamiliarRESUMEN
The Turner syndrome (TS) is a complex disorder associated with almost invariant short stature and gonadal dysgenesis, as well as a variety of other major organ malformations. Recently, a homeobox-containing gene entitled short-stature homeobox-containing gene (SHOX), was isolated from a minimal short stature gene interval from the pseudoautosomal region of Xp (and Yp). Together with the demonstrable escape of SHOX from X-inactivation, this suggested SHOX to be a strong candidate gene for the short stature component of TS, and as SHOX haploinsufficiency appears to be the molecular basis of a mesomelic short statured skeletal dysplasia (Leri-Weill syndrome), this suggested that SHOX protein expression levels may confer a dosage effect on human stature. However, in this communication we report a normal statured female with gonadal dysgenesis, due to the inheritance of a recombinant duplication-deletion X-chromosome. The karyotype of the proband was 46,X,rec(X)dup(Xp)inv(X)(p11.22q21.2)mat and fluorescent in situ hybridization of her metaphases with a SHOX cosmid confirmed the proband to be trisomic for SHOX. This communication suggests the relationship between levels of SHOX expression and human stature to be more complex than envisaged previously. The presence of normal stature in our patient rather than tall stature is likely to represent the natural variation seen in patients with transcription factor disorders.
Asunto(s)
Estatura/genética , Disgenesia Gonadal 46 XX/genética , Proteínas de Homeodominio/genética , Trisomía , Cromosoma X/genética , Adolescente , Compensación de Dosificación (Genética) , Terapia de Reemplazo de Estrógeno , Femenino , Disgenesia Gonadal 46 XX/tratamiento farmacológico , Humanos , Hibridación Fluorescente in Situ , Proteína de la Caja Homeótica de Baja EstaturaRESUMEN
Compared to other regions on the human Y chromosome, the genomic segment encompassing the functionally defined AZFa locus has undergone higher X-Y sequence divergence, which is detectable by fluorescence in-situ hybridisation. This allows an evolutionary definition of an interval enclosing AZFa with a size of about 1.1 Mb. The region includes the genes USP9Y, DBY and UTY and is limited by evolutionary breakpoints within the PAC clones 41L06 and 46M11. These breakpoints restrict an area of possible male specific evolution that may have resulted in the acquisition of male specific functions, including a role in spermatogenesis.
Asunto(s)
Cromosomas Humanos Y/genética , Oligospermia/genética , Células Cultivadas , Cromosomas Humanos X/genética , Mapeo Contig , Evolución Molecular , Humanos , Hibridación Fluorescente in Situ , Masculino , Microscopía FluorescenteRESUMEN
Functional impairment of the human homeobox gene SHOX causes short stature and Madelung deformity in Leri-Weill syndrome (LWS) and has recently been implicated in additional skeletal malformations frequently observed in Turner syndrome. To enhance our understanding of the underlying mechanism of action, we have established a cell culture model consisting of four stably transfected cell lines and analysed the functional properties of the SHOX protein on a molecular level. Results show that the SHOX-encoded protein is located exclusively within the nucleus of a variety of cell lines, including U2Os, HEK293, COS7 and NIH 3T3 cells. In contrast to this cell-type independent nuclear translocation, the transactivating potential of the SHOX protein on different luciferase reporter constructs was observed only in the osteogenic cell line U2Os. Since C-terminally truncated forms of SHOX lead to LWS and idiopathic short stature, we have compared the activity of wild-type and truncated SHOX proteins. Interestingly, C-terminally truncated SHOX proteins are inactive with regards to target gene activation. These results for the first time provide an explanation of SHOX-related phenotypes on a molecular level and suggest the existence of qualitative trait loci modulating SHOX activity in a cell-type specific manner.
Asunto(s)
Proteínas de Homeodominio/genética , Transactivadores/genética , Western Blotting , Estatura , Línea Celular , Clonación Molecular , Proteínas de Unión al ADN/genética , Técnica del Anticuerpo Fluorescente , Genes Homeobox , Proteínas de Homeodominio/fisiología , Humanos , Proteína de la Caja Homeótica de Baja Estatura , Transactivadores/fisiología , Síndrome de Turner/embriología , Síndrome de Turner/genética , Síndrome de Turner/fisiopatología , Técnicas del Sistema de Dos HíbridosRESUMEN
We report on a three-month-old boy with a 46,XY,der(Y)t(Y;7)(p11.32;p15.3) karyotype and growth deficiency, postnatal microcephaly with large fontanels, wide sagittal and metopic sutures, hypertelorism, choanal stenosis, micrognathia, bilateral cryptorchidism, hypospadias, abnormal fingers and toes, and severe developmental delay. FISH studies showed partial trisomy 7p resulting from a de novo unbalanced translocation. The application of molecular probes from the TWIST gene region (7p15.3-p21.1) and probes from the pseudoautosomal region (PAR) demonstrated that the 7p15.3-pter fragment was translocated onto Yp with the breakpoint within approximately 20 kb from the Yp telomere. We discuss the possible role of the TWIST gene in abnormal skull development and suggest that trisomy 7p cases with delayed closure of fontanels can be a result of TWIST gene dosage effect.
Asunto(s)
Cromosomas Humanos Par 7/genética , Proteínas Nucleares , Factores de Transcripción/genética , Trisomía , Anomalías Múltiples/genética , Anomalías Múltiples/patología , Adolescente , Niño , Dedos/anomalías , Trastornos del Crecimiento/patología , Humanos , Hibridación Fluorescente in Situ , Lactante , Cariotipificación , Masculino , Microcefalia/patología , Fenotipo , Dedos del Pie/anomalías , Translocación Genética , Proteína 1 Relacionada con Twist , Cromosoma Y/genéticaRESUMEN
Serotonin receptor type 3 is a ligand-gated ion channel implicated in behavioural disorders. Our objective was to identify nucleotide variants in a specific portion of the 5' region of the serotonin receptor gene (HTR3A) containing upstream open reading frames (uORFs) and to investigate their effect on bipolar disease. Mutations in uORFs have been recently shown to cause disease by changing expression on the translational level. We identified one polymorphism, C195T, and one missense mutation, C178T (Pro16Ser) within an upstream open reading frame. No significant association was found between the C195T polymorphism and bipolar affective disorder. A significant association was, however, found between the variant C178T in 156 patients with bipolar disorder compared to 156 healthy controls (P = 0.00016). To investigate the relevance of this variant on gene expression, luciferase reporter constructs containing the C178T (Pro16Ser) allele were established and compared to the C178T plus C195T and wild-type alleles. Reporter constructs containing the C178T (Pro16Ser) allele drove 245% and 138% expression compared to the wild-type allele. These findings show that the C178T(Pro16Ser) variant in HTR3A may represent a functional variant and affect the susceptibility to bipolar disorder.
Asunto(s)
Regiones no Traducidas 5'/genética , Trastorno Bipolar/genética , Receptores de Serotonina/genética , Frecuencia de los Genes , Humanos , Polimorfismo Genético , Polimorfismo de Nucleótido Simple , Polimorfismo Conformacional Retorcido-Simple , Receptores de Serotonina 5-HT3RESUMEN
Linear growth is a multifactorial trait that is influenced and regulated by a combination of environmental and internal factors. Among the intrinsic determinants of final body height, genetic factors have become more and more prominent, and the list of genes involved in growth-related processes has been extended accordingly. One of the most exciting additions to this list is represented by the discovery of the pseudoautosomal gene SHOX. Originally described as a gene responsible for idiopathic short stature, it has become clear that SHOX mutations can also cause mesomelic short stature and Madelung deformity in Léri-Weill syndrome. In addition, recent studies implicate SHOX haploinsufficiency in a variety of somatic Turner syndrome stigmata.
Asunto(s)
Estatura/genética , Trastornos del Crecimiento/genética , Proteínas de Homeodominio/genética , Mutación/fisiología , Clonación Molecular , Humanos , Osteocondrodisplasias/genética , Proteína de la Caja Homeótica de Baja Estatura , Síndrome , Síndrome de Turner/genéticaRESUMEN
We report the results of detailed molecular-cytogenetic studies of two isodicentric Y [idic(Y)] chromosomes identified in patients with complex mosaic karyotypes. We used fluorescence in situ hybridization (FISH) and polymerase chain reaction (PCR) to determine the structure and genetic content of the abnormal chromosomes. In the first patient, classical cytogenetics and FISH analysis with Y chromosome-specific probes showed in peripheral blood lymphocytes a karyotype with 4 cell lines: 45,X[128]/46,X,+idic(Y)(p11.32)[65]/47,XY,+idic(Y)(p11.32)[2]/47,X,+2idic(Y)(p11.32)[1]. No Y chromosome material was found in the removed gonads. For precise characterization of the Yp breakpoint, FISH and fiberFISH analysis, using a telomeric probe and a panel of cosmid probes from the pseudoautosomal region PAR1, was performed. The results showed that the breakpoint maps approximately 1,000 Kb from Ypter. The second idic(Y) chromosome was found in a boy with mild mental retardation, craniofacial anomalies, and the karyotype in lymphocytes 47,X,+idic(Y)(q11.23),+i(Y)(p10)[77]/46,X,+i(Y)(p10)[23]. To our knowledge, such an association has not been previously described. FISH and PCR analysis indicated the presence of at least two copies of the SRY gene in all analyzed cells. Using 17 PCR primers, the Yq breakpoint was shown to map between sY123 (DYS214) and sY121 (DYS212) loci in interval 5O in AZFb region. Possible mechanisms of formation of abnormal Y chromosomes and karyotype-phenotype correlations are discussed.