RESUMO
BACKGROUND: A marker chromosome is defined as a structurally abnormal chromosome that cannot be identified by routine cytogenetics. The risk for phenotypic abnormalities associated with a marker chromosome depends on several factors, including inheritance, mode of ascertainment, chromosomal origin, and the morphology, content, and structure of the marker. METHODS: to understand the karyotype-phenotype relationship of prenatally ascertained supernumerary de novo marker chromosomes, we combined data from prenatal cases obtained from 12 laboratories with those from studies in the literature. We were able to obtain cytogenetic and phenotypic data from 108 prenatally ascertained supernumerary de novo marker chromosomes to refine the phenotypic risk associated with these markers. Because of the growing number of cases and because more techniques are available to delineate marker morphology, we have been able to group risk estimates into subcategories, such as by marker type and whether there are ultrasound abnormalities. RESULTS: If a de novo supernumerary marker chromosome is found prenatally, our data suggest there is a 26% risk for phenotypic abnormality when there is no other information defining the marker (such as chromosomal origin or information about the existing phenotype). However, if high resolution ultrasound studies are normal, this risk reduces to 18%. CONCLUSIONS: Our findings strongly support the value of additional genetic studies for more precisely defining the risk in individual cases involving marker chromosomes.
Assuntos
Aberrações Cromossômicas , Comportamento Cooperativo , Diagnóstico Pré-Natal , Feminino , Humanos , Fenótipo , Gravidez , Fatores de RiscoRESUMO
A patient with dir dup 2(q37.1q33.1) is described. Literature review of chromosome 2q duplications suggests a consistent, though nonspecific, facial phenotype. Segregation of those cases that are "pure" duplications from those with accompanying monosomy for another chromosome suggests that a cleft palate may not be attributable to the duplicated segment.
Assuntos
Aberrações Cromossômicas , Cromossomos Humanos Par 2/genética , Adolescente , Adulto , Criança , Pré-Escolar , Bandeamento Cromossômico , Feminino , Duplicação Gênica , Humanos , Lactente , Recém-Nascido , Masculino , Pessoa de Meia-IdadeRESUMO
Supernumerary ring chromosomes varying with respect to both size and number were found as the primary cytogenetic anomaly in a rare benign soft tissue chondroma resected from the floor of the mouth of a 3-year-old girl. Reverse fluorescence in situ hybridization paint probes prepared by polymerase chain reaction from microdissected rings produced fluorescent signal over two large but discontinuous parts of the chromosome 12 long arm, subdivided into four regions. This case expands the spectrum of mesenchymal neoplasms in which ring chromosomes have been described as the primary genetic anomaly. A review of the literature reporting similar findings in other soft tissue tumors further supports the possibility that low-level amplification of chromosome 12 long-arm regions may contribute to abnormal cellular proliferation in a variety of mesenchymal tumors. Genes implicated in the control of the cell cycle such as sarcoma amplified sequence (SAS), the human homolog of the murine double-minute type 2 gene (MDM-2), proto-oncogenes CHOP/GADD153, GLI, A2MR, cyclin-dependent kinase (CDK4), and the high mobility group (HMGIC) gene implicated in mesenchymal tumorigenesis are all located on the long arm of chromosome 12. Chromosomal abnormalities involving the 12q13-q15 region are associated with a wide range of benign soft tissue tumors and sarcomas.
Assuntos
Condroma/genética , Cromossomos Humanos Par 12 , Neoplasias Bucais/genética , Cromossomos em Anel , Pré-Escolar , Condroma/patologia , Feminino , Humanos , Hibridização in Situ Fluorescente , Cariotipagem , Neoplasias Bucais/patologiaRESUMO
The physical and genetic characterization of a stable human minichromosome in a Chinese hamster hybrid cell is described. The minichromosome is 2-3 Mb in size, is linear, and contains a complementing SDHC gene. It is derived from a human chromosome 1, including the centromere, some pericentric heterochromatin from 1q12, and 1-2 Mb of 1q21. Genomic DNA surrounding the SDHC gene was used to construct a targeting vector with a selectable drug resistance marker (neo(R)); the marker was then successfully integrated into the minichromosome. With the new selectable marker, the 8.2.3 minichromosome could be transferred into mouse LMTK(-) and 3T3 TK(-) cells.
Assuntos
Cromossomos Humanos Par 1 , Cromossomos Humanos , Succinato Desidrogenase/genética , Animais , Reanimação Cardiopulmonar , Linhagem Celular , Mapeamento Cromossômico , Cricetinae , Cricetulus , Eletroforese em Gel de Campo Pulsado , Técnicas de Transferência de Genes , Humanos , Células Híbridas , Hibridização in Situ Fluorescente , Cariotipagem , Células L , Camundongos , Timidina Quinase/deficiência , Timidina Quinase/genéticaRESUMO
Vertebrates have four clusters of Hox genes (HoxA, HoxB, HoxC, and HoxD). A variety of expression and mutation studies indicate that posterior members of the HoxA and HoxD clusters play an important role in vertebrate limb development. In humans, mutations in HOXD13 have been associated with type II syndactyly or synpolydactyly, and, in HOXA13, with hand-foot-genital syndrome. We have investigated two unrelated children with a previously unreported pattern of severe developmental defects on the anterior-posterior (a-p) limb axis and in the genitalia, consisting of a single bone in the zeugopod, either monodactyly or oligodactyly in the autopod of all four limbs, and penoscrotal hypoplasia. Both children are heterozygous for a deletion that eliminates at least eight (HOXD3-HOXD13) of the nine genes in the HOXD cluster. We propose that the patients' phenotypes are due in part to haploinsufficiency for HOXD-cluster genes. This hypothesis is supported by the expression patterns of these genes in early vertebrate embryos. However, the involvement of additional genes in the region could explain the discordance, in severity, between these human phenotypes and the milder, non-polarized phenotypes present in mice hemizygous for HoxD cluster genes. These cases represent the first reported examples of deficiencies for an entire Hox cluster in vertebrates and suggest that the diploid dose of human HOXD genes is crucial for normal growth and patterning of the limbs along the anterior-posterior axis.
Assuntos
Proteínas de Ligação a DNA , Proteínas de Homeodomínio/genética , Deformidades Congênitas dos Membros/genética , Fatores de Transcrição , Pré-Escolar , Cromossomos Humanos Par 2 , Deleção de Genes , Dosagem de Genes , Marcadores Genéticos , Genitália Masculina/anormalidades , Humanos , Recém-Nascido , Deformidades Congênitas dos Membros/diagnóstico por imagem , Masculino , Dados de Sequência Molecular , Família Multigênica , RadiografiaRESUMO
Complex II of mitochondria contains succinate dehydrogenase and subunits to link this enzyme directly to the inner mitochondrial membrane. The four peptides of this complex are the flavoprotein (Fp) and iron-sulfur protein (Ip) of the dehydrogenase, and two integral membrane proteins referred to as C(II-3) and C(II-4). Their respective genes in mammals are SDHA, SDHB, SDHC and SDHD) in order of decreasing molecular weights of the peptides. In this paper we describe the identification of two pseudogenes and the complete characterization and mapping of the active SDHC gene in humans. The active gene, encoding a small peptide of 15.5 kDa, has six exons and five introns extending over 35 kb. It has been mapped at position 1q21, adjacent to the pericentric heterochromatin on the long arm of chromosome 1. Approximately I kb of the promoter region has also been sequenced and examined for sequence motifs suggesting the binding of known transcription factors. Several potential sites for the nuclear respiratory factors NRF-1 and NRF-2 were identified.
Assuntos
Cromossomos Humanos Par 1/genética , Genes , Proteínas de Membrana/genética , Sequência de Aminoácidos , Animais , Sequência de Bases , Sítios de Ligação , Bovinos , Mapeamento Cromossômico , Proteínas de Ligação a DNA/metabolismo , Éxons , Fator de Transcrição de Proteínas de Ligação GA , Biblioteca Gênica , Humanos , Hibridização in Situ Fluorescente , Íntrons , Mitocôndrias/enzimologia , Dados de Sequência Molecular , Fator 1 Relacionado a NF-E2 , Fator 1 Nuclear Respiratório , Fatores Nucleares Respiratórios , Regiões Promotoras Genéticas , Pseudogenes , Alinhamento de Sequência , Homologia de Sequência do Ácido Nucleico , Transativadores/metabolismo , Fatores de Transcrição/metabolismoRESUMO
A female patient with the karyotype 45,X/46, X, r(X)(p11.2 q13) and severe developmental delay, prominent fingertip pads, long palpebral fissures, short stature, and history of hypotonia had a phenotype reminiscent of Kabuki syndrome. We hypothesized that overexpression of X chromosome-derived sequences might be associated with the Kabuki-like phenotype observed. The nature and parental origin of this small-ring X were ascertained using a combination of genotyping with microsatellite markers and quantitative Southern blotting. PCR-based genotyping demonstrated heterozygosity at X-linked loci SBMA (Xq11-q12) and DXS227 (Xq13.1). Hemizygosity was observed at several loci: DMD STR-49 (Xp21.2), DXS1003 (Xp11.23), DXS988 (Xp11.21), DXS101 (Xq21.3), FMR-1 (Xq27.3), and DXYS64 (Xq28). This ring X chromosome is paternally derived since only maternal alleles are inherited at three informative microsatellite loci. Results of FISH and RT-PCR experiments indicate that the XIST locus is missing in the ring X chromosome and not expressed. These data indicated a large deletion of the X chromosome consistent with a small-ring X chromosome with approximate breakpoints near p11.2 and q13. These results are comparable to the observation of others where an atypically severe phenotype has been associated with the presence of an r(X), or small mar(X).
Assuntos
Anormalidades Múltiplas/genética , Face/anormalidades , Cromossomos em Anel , Cromossomo X , Criança , Mapeamento Cromossômico , Feminino , Marcadores Genéticos , Impressão Genômica , Genótipo , Heterozigoto , Humanos , Cariotipagem , Masculino , Repetições de Microssatélites , Reação em Cadeia da PolimeraseRESUMO
We introduce a new epithelial ovarian carcinoma cell line (UCI 107) from a patient with papillary adenocarcinoma of the ovary who had not been previously treated. The growth characteristics, chemosensitivity, tumorgenicity, cytogenetics, antigen expression, and receptor status were examined. A standardized photometric assay was implemented to determine the response to single drug agents including doxorubicin (ADR), cisplatin (CDDP), and Taxol. Tumorgenicity was determined utilizing female athymic mice implanted either subcutaneously (sc) or intraperitoneally (ip) with 1 x 10(7) UCI 107 cells. UCI 107 cells grow rapidly in culture with lag phase of approximately 48 hr, population doubling time of 24-36 hr, and saturation density of 4.8 x 10(5) cells/cm2. The 50% inhibitory concentration values for the chemotherapeutic agents were 0.170, 0.029, and 0.330 microM for ADR, Taxol, and CDDP, respectively. Nude mice produced ip tumors within 15 days, resulting in death from carcinomatosis 40-45 days postimplantation. Subcutaneous tumor nodules (100 mm3) were observed in nude mice 12-13 days post-tumor implantation reaching a maximum tumor volume of approximately 10,000 mm3 by Day 30. The cytogenetic composite karyotype is as follows: 46, X, der (X) t (X;7) (p11;q22), inv dup (1) (q12;q32), t (6;6;11;22) (p21.3;q16;q23.3;q13.3), del (13) (q14.1). The cell line expresses progesterone receptor, increased levels of p53 protein, and cytokeratins. It does not appear to express Her-2/neu protein, estrogen receptor, nor the CA 125 tumor marker. In conclusion, UCI 107 displays unique cellular properties which make it an attractive model for the study of ovarian cancer.
Assuntos
Carcinoma/patologia , Neoplasias Ovarianas/patologia , Animais , Antígenos de Neoplasias/metabolismo , Carcinoma/genética , Divisão Celular , Mapeamento Cromossômico , Feminino , Humanos , Camundongos , Camundongos Nus , Pessoa de Meia-Idade , Transplante de Neoplasias , Neoplasias Ovarianas/genética , Receptores de Superfície Celular/metabolismo , Transplante Heterólogo , Células Tumorais CultivadasRESUMO
Squamous carcinoma of the vulva (SCV) is an uncommon neoplasm of uncertain etiology. There is evidence that there are two subgroups of SCV, one associated with human papilloma virus (HPV) and a second HPV-negative group. The UCI-VULV-1 cell line, obtained from a lymph node metastasis of an SCV, grows with a population doubling time of approximately 60 hr. The saturation density is 10(5) cells/cm2. The cell line does not exhibit anchorage independence and is weakly tumorigenic. The cells range in appearance from an abundant spindle cell to a less common larger, flat cell. All of the cells are immunoreactive for high-molecular-weight keratin, but only the flat cells, which form squamous pearls in vivo, are immunoreactive for low-molecular-weight keratin. The cell line expresses epidermal growth factor (EGF), transforming growth factor-alpha, the EGF receptor, and p53 protein. Polymerase chain reaction revealed no HPV DNA within the cells. Early passage cells exhibited karyotypic heterogeneity with few similarities to previous described SCV karyotypes. The cells display sensitivity to cis-platinum in concentrations toxic to many ovarian and cervical carcinoma lines. UCI-VULV-1 may be helpful for studying the properties of the HPV-negative form of SCV.
Assuntos
Carcinoma de Células Escamosas/patologia , Células Tumorais Cultivadas , Neoplasias Vulvares/patologia , Idoso , Divisão Celular , Sondas de DNA de HPV , Feminino , Humanos , Cariotipagem , Células Tumorais Cultivadas/patologia , Células Tumorais Cultivadas/virologiaRESUMO
Injecting male embryonic stem cells into the blastocoel of female embryos occasionally produces female chimeras capable of transmitting the embryonic stem cell genome. In our experiments several embryonic stem cell-derived male offspring from female chimeras were observed to be infertile. Karyotypic analysis of these infertile animals revealed aneuploidy. We examined the karyotypes of an additional 14 offspring not selected for infertility (3 females and 11 males) that had received the embryonic stem cell genome from 5 transmitting female chimeras. The 3 females and 5 of the males had normal karyotypes. Six of the males exhibited nonmosaic aneuploidy, which included four XXY karyotypes, one XYY karyotype, and an X,i(Y) karyotype. The high incidence of XXY and XYY males supports previous evidence for aberrant pairing and segregation of X and Y chromosomes when they are present in oocytes.
Assuntos
Aneuploidia , Aberrações dos Cromossomos Sexuais , Diferenciação Sexual/genética , Transplante de Células-Tronco , Quimeras de Transplante , Animais , Transplante de Células , Bandeamento Cromossômico , Feminino , Infertilidade Masculina , Cariotipagem , Síndrome de Klinefelter , Masculino , Meiose , Camundongos , Camundongos Endogâmicos C57BL , Cariótipo XYYRESUMO
Fluorescence in situ hybridization utilizing a probe for the alpha satellite repeat sequence on chromosome 11 was used to detect variations in the number of chromosomes 11 in 24 formalin-fixed, paraffin-embedded congenital mesoblastic nephromas. Evidence of trisomy 11 was found in nearly half of the tumors. More importantly, the presence of trisomy 11 was associated with the cellular histologic variant of this tumor.
Assuntos
Cromossomos Humanos Par 11 , Neoplasias Renais/genética , Nefroma Mesoblástico/complicações , Nefroma Mesoblástico/genética , Trissomia , Humanos , Hibridização in Situ Fluorescente , Neoplasias Renais/patologia , Nefroma Mesoblástico/patologiaRESUMO
We report the detection of a mosaic triple trisomy, 46,XY/49,XY,+13,+20,+21, in two amniotic fluid specimens obtained from a pregnancy that yielded a normal infant. Traditional cytogenetic methods failed to detect the abnormal cell lineage in fetal blood, foreskin, amnion, umbilical cord, and three different biopsies of the chorion. In addition, fluorescence in situ hybridization study of cells from a buccal smear showed no evidence of cells with three copies of chromosome 20.
Assuntos
Cromossomos Humanos Par 13 , Cromossomos Humanos Par 20 , Cromossomos Humanos Par 21 , Feto/fisiologia , Mosaicismo , Trissomia , Amniocentese , Âmnio/citologia , Células Cultivadas , Feminino , Humanos , Cariotipagem , Masculino , Fenótipo , Gravidez , Valores de ReferênciaRESUMO
We present the case of a 14-year-old girl in whom a myelodysplastic syndrome was diagnosed 9 months after surgical resection and chemotherapy for an ovarian germ cell tumor. Cells from her marrow were characterized by trisomy 8 and an isochromosome 12p, a marker that appears to be unique to germ cell tumors. The presence of the same two anomalies in her original tumor was demonstrated by fluorescence in situ hybridization study of interphase cells in paraffin-embedded tissues and thus provided strong evidence that the two neoplasms had a common clonal origin.
Assuntos
Síndromes Mielodisplásicas/etiologia , Neoplasias Embrionárias de Células Germinativas/genética , Neoplasias Ovarianas/genética , Adolescente , Bandeamento Cromossômico , Cromossomos Humanos Par 12 , Cromossomos Humanos Par 8 , Células Clonais , Terapia Combinada , Feminino , Humanos , Cariotipagem , Neoplasias Embrionárias de Células Germinativas/complicações , Neoplasias Embrionárias de Células Germinativas/tratamento farmacológico , Neoplasias Embrionárias de Células Germinativas/cirurgia , Neoplasias Ovarianas/complicações , Neoplasias Ovarianas/tratamento farmacológico , Neoplasias Ovarianas/cirurgia , TrissomiaRESUMO
We report results of the first cytogenetic study of an osteoblastoma. Cells from the tumor were characterized by a three-way unbalanced translocation involving chromosomes 15, 17, and 20. As a consequence of the translocation, most of one chromosome 17 short arm appears to have been lost. This loss suggests the possibility that loss of 17p DNA sequences may be involved in early changes leading to neoplastic proliferation of osteoblasts.
Assuntos
Neoplasias Ósseas/genética , Deleção Cromossômica , Cromossomos Humanos Par 17 , Osteoma Osteoide/genética , Translocação Genética , Neoplasias Ósseas/diagnóstico por imagem , Neoplasias Ósseas/patologia , Criança , Cromossomos Humanos Par 15 , Cromossomos Humanos Par 20 , Humanos , Cariotipagem , Masculino , Osteoma Osteoide/diagnóstico por imagem , Osteoma Osteoide/patologia , Tomografia Computadorizada por Raios XRESUMO
We report the karyotype analysis of a congenital mesoblastic nephroma (CMN), a usually benign renal tumor occurring most commonly during early infancy. The tumor was composed of interlacing bundles of spindle-shaped cells and it displayed both the classic and cellular histologic patterns. Immunoperoxidase studies showed reactivity for vimentin and actin. The tumor cell karyotype included additional chromosomes 11 and an altered chromosome 12. Trisomy or tetrasomy of chromosome 11 is present in five of six reported cases and may represent a frequent alteration in the karyotype of the CMN. Furthermore, breakpoints in the q13-15 region of chromosome 12 are commonly seen in leiomyomas, which are histologically similar to the CMN. Thus, the karyotype described here illustrates another similarity between the two tumor types.
Assuntos
Aberrações Cromossômicas/genética , Cromossomos Humanos Par 11 , Cromossomos Humanos Par 12 , Neoplasias Renais/genética , Tumor de Wilms/genética , Transtornos Cromossômicos , Feminino , Humanos , Recém-Nascido , Cariotipagem , Neoplasias Renais/congênito , Neoplasias Renais/patologia , Leiomioma/genética , Tumor de Wilms/congênito , Tumor de Wilms/patologiaRESUMO
Cytogenetic study of a mesenchymal hamartoma of the liver detected a balanced translocation between chromosomes 11 and 19 in a 6-month-old male whose constitutional karyotype was normal. The chromosome 19 breakpoint, 19q13.4, appears to be identical to one of the breakpoints identified in the only other mesenchymal hamartoma studied with cytogenetic methods.
Assuntos
Cromossomos Humanos Par 19 , Hamartoma/genética , Hamartoma/patologia , Neoplasias Hepáticas/genética , Neoplasias Hepáticas/patologia , Translocação Genética , Bandeamento Cromossômico , Cromossomos Humanos Par 11 , Seguimentos , Hamartoma/diagnóstico por imagem , Hamartoma/cirurgia , Humanos , Lactente , Cariotipagem , Neoplasias Hepáticas/diagnóstico por imagem , Neoplasias Hepáticas/cirurgia , Imageamento por Ressonância Magnética , Masculino , Células Tumorais Cultivadas , UltrassonografiaRESUMO
We report on an 11-year experience in which cell culture synchronization and other methods for improving cytogenetic detail were used to study 2,245 patients presenting with malformations and (usually) developmental delay. Not including patients presenting with one of the so-called "contiguous gene syndromes," 30 patients (1.1% of the study population) were found to have karyotypes characterized by structural alterations that were either subtle enough to be judged undetectable in standard metaphase preparations or subtle enough to have escaped detection in previous banded studies. Analysis of the detail available for 6 chromosome pairs suggests that the average banding detail available for these analyses fell short of that considered to be "high-resolution" but was, nevertheless, more than would have been expected from standard metaphase preparations.
Assuntos
Bandeamento Cromossômico , Anormalidades Congênitas/diagnóstico , Feminino , Humanos , Cariotipagem , MasculinoRESUMO
Karyotypic study of two hepatoblastomas revealed trisomies for chromosome 20 and the presence of double minutes (dmin). These cases are the second and third examples of trisomy 20 in hepatoblastoma and are the first examples of dmins in this rare childhood tumor.
Assuntos
Carcinoma Hepatocelular/genética , Cromossomos Humanos Par 20 , Neoplasias Hepáticas/genética , Trissomia , Humanos , Lactente , Cariotipagem , MasculinoRESUMO
Multiple inserted duplications of bands 3q21 through 3q27 and a duplication of the chromosome 1 long arm are reported in a karyotypically altered clone from a dysmorphic child with myelodysplasia.
Assuntos
Aberrações Cromossômicas , Cromossomos Humanos Par 1 , Cromossomos Humanos Par 3 , Síndromes Mielodisplásicas/genética , Adolescente , Feminino , HumanosRESUMO
We describe a chromosome 22 deletion in a patient with the DiGeorge malformation sequence as manifested by an interrupted aortic arch, mild thymic hypoplasia, and minor craniofacial anomalies. Although others have reported DiGeorge sequence patients with deletions derived from unbalanced translocations involving the chromosome 22 long arm, the small interstitial deletion described here appears to be unusual for patients with this disorder.