RESUMEN
BACKGROUND: In 1993, Chitayat et al., reported a newborn with hyperphalangism, facial anomalies, and bronchomalacia. We identified three additional families with similar findings. Features include bilateral accessory phalanx resulting in shortened index fingers; hallux valgus; distinctive face; respiratory compromise. OBJECTIVES: To identify the genetic aetiology of Chitayat syndrome and identify a unifying cause for this specific form of hyperphalangism. METHODS: Through ongoing collaboration, we had collected patients with strikingly-similar phenotype. Trio-based exome sequencing was first performed in Patient 2 through Deciphering Developmental Disorders study. Proband-only exome sequencing had previously been independently performed in Patient 4. Following identification of a candidate gene variant in Patient 2, the same variant was subsequently confirmed from exome data in Patient 4. Sanger sequencing was used to validate this variant in Patients 1, 3; confirm paternal inheritance in Patient 5. RESULTS: A recurrent, novel variant NM_006494.2:c.266A>G p.(Tyr89Cys) in ERF was identified in five affected individuals: de novo (patient 1, 2 and 3) and inherited from an affected father (patient 4 and 5). p.Tyr89Cys is an aromatic polar neutral to polar neutral amino acid substitution, at a highly conserved position and lies within the functionally important ETS-domain of the protein. The recurrent ERF c.266A>C p.(Tyr89Cys) variant causes Chitayat syndrome. DISCUSSION: ERF variants have previously been associated with complex craniosynostosis. In contrast, none of the patients with the c.266A>G p.(Tyr89Cys) variant have craniosynostosis. CONCLUSIONS: We report the molecular aetiology of Chitayat syndrome and discuss potential mechanisms for this distinctive phenotype associated with the p.Tyr89Cys substitution in ERF.
Asunto(s)
Anomalías Múltiples/genética , Síndrome de Dandy-Walker/genética , Discapacidades del Desarrollo/genética , Huesos Faciales/anomalías , Proteínas Represoras/genética , Anomalías Múltiples/fisiopatología , Broncomalacia/genética , Broncomalacia/fisiopatología , Síndrome de Dandy-Walker/fisiopatología , Discapacidades del Desarrollo/fisiopatología , Exoma/genética , Cara/fisiopatología , Huesos Faciales/fisiopatología , Femenino , Hallux Valgus/genética , Hallux Valgus/fisiopatología , Secuenciación de Nucleótidos de Alto Rendimiento , Humanos , Recién Nacido , Masculino , FenotipoRESUMEN
Neurofibromatosis type 1 (NF1) is a commonly inherited autosomal dominant disorder. Previous studies indicated that mice homozygous for a null mutation in Nf1 exhibit mid-gestation lethality, whereas heterozygous mice have an increased predisposition to tumors and learning impairments. Here we show that mice lacking the alternatively spliced exon 23a, which modifies the GTPase-activating protein (GAP) domain of Nf1, are viable and physically normal, and do not have an increased tumor predisposition, but show specific learning impairments. Our findings have implications for the development of a treatment for the learning disabilities associated with NF1 and indicate that the GAP domain of NF1 modulates learning and memory.
Asunto(s)
Exones , Predisposición Genética a la Enfermedad , Discapacidades para el Aprendizaje/genética , Neoplasias Experimentales/genética , Animales , Secuencia de Bases , Cartilla de ADN , Genes de Neurofibromatosis 1 , Ratones , Neurofibromatosis 1/genética , Reacción en Cadena de la Polimerasa de Transcriptasa InversaRESUMEN
Disorders of the Ras/mitogen-activated protein kinase (MAPK) pathway have an overlapping skeletal phenotype (e.g. scoliosis, osteopenia). The Ras proteins regulate cell proliferation and differentiation and neurofibromatosis type 1 (NF1) individuals have osteoclast hyperactivity and increased bone resorption as measured by urine pyridinium crosslinks [pyridinoline (Pyd) and deoxypyridinoline (Dpd)]. Pyd and Dpd are hydroxylysine-derived crosslinks of collagen found in bone and cartilage and excreted in the urine. Dpd is most abundant in bone. The aim of this study was to evaluate if other syndromes of the Ras/MAPK pathway have increased bone resorption, which may impact the skeletal phenotype. Participants were individuals with Noonan syndrome (n = 14), Costello syndrome (n = 21), and cardiofaciocutaneous (CFC) syndrome (n = 14). Pyridinium crosslinks from two consecutive first morning urines were extracted after acid hydrolysis and analyzed by high performance liquid chromatography. Three separate analyses of covariance were performed to compare Pyd, Dpd, and Dpd/Pyd ratio of each group to controls after controlling for age. Data were compared to 99 healthy controls. The Dpd and the Dpd/Pyd ratio were elevated (p < 0.0001) in all three conditions compared to controls suggesting that collagen degradation was predominantly from bone. The data suggest that the Ras/MAPK signal transduction pathway is important in bone homeostasis.
Asunto(s)
Resorción Ósea/patología , Sistema de Señalización de MAP Quinasas , Proteínas Proto-Oncogénicas p21(ras)/genética , Transducción de Señal , Absorciometría de Fotón , Adolescente , Adulto , Aminoácidos/orina , Biomarcadores/orina , Densidad Ósea , Resorción Ósea/genética , Resorción Ósea/orina , Estudios de Casos y Controles , Niño , Preescolar , Cromatografía Líquida de Alta Presión , Estudios de Cohortes , Colágeno/orina , Síndrome de Costello/genética , Síndrome de Costello/patología , Síndrome de Costello/orina , Análisis Mutacional de ADN , Displasia Ectodérmica/genética , Displasia Ectodérmica/patología , Displasia Ectodérmica/orina , Facies , Insuficiencia de Crecimiento/genética , Insuficiencia de Crecimiento/patología , Insuficiencia de Crecimiento/orina , Femenino , Pruebas Genéticas , Cardiopatías Congénitas/genética , Cardiopatías Congénitas/patología , Cardiopatías Congénitas/orina , Humanos , Hidrólisis , Masculino , Síndrome de Noonan/genética , Síndrome de Noonan/patología , Síndrome de Noonan/orina , Proteína Tirosina Fosfatasa no Receptora Tipo 11/genética , Adulto JovenRESUMEN
BACKGROUND: The role of germline and somatic SMARCB1 gene mutations in malignant rhabdoid tumour (MRT) predisposition is well known. Germline SMARCB1 mutations have also recently been identified in a subset of individuals with schwannomatosis. Surprisingly, MRT predisposition and schwannomatosis have never been reported to co-occur in a family. The correlation between genotype and phenotype for mutations in SMARCB1 has not been determined. RESULTS: We have identified a germline 2631 bp duplication that includes exon 6 of SMARCB1 in a unique family with a four generation history of MRT predisposition and schwannomatosis. This duplication segregates with disease in individuals affected with both conditions, linking MRT predisposition and schwannomatosis as components of the same syndrome in this family. CONCLUSION: The unique combination of tumours that result from the duplication described in this report may provide important clues about the mechanisms that influence the phenotype associated with a given SMARCB1 mutation.
Asunto(s)
Proteínas Cromosómicas no Histona/genética , Proteínas de Unión al ADN/genética , Duplicación de Gen , Neurilemoma/genética , Tumor Rabdoide/genética , Factores de Transcripción/genética , Secuencia de Bases , Exones , Familia , Genotipo , Mutación de Línea Germinal , Humanos , Datos de Secuencia Molecular , Neurilemoma/patología , Linaje , Fenotipo , Tumor Rabdoide/patología , Proteína SMARCB1RESUMEN
Skeletal anomalies are observed in neurofibromatosis type 1 (NF1), but the pathogenesis is unknown. Given that muscle mass is important in the development of the strength of bone, peripheral quantitative computed tomography (pQCT) was utilized to compare measurements of muscle compartments between NF1 individuals and controls. Forty individuals with NF1 (age 5-18 years) were evaluated. Cross-sectional measurements, at the 66% tibial site, were obtained using pQCT (XCT-2000, Stratec) and variables were compared to controls without NF1 ((age 5-18 years, N=380) using analysis-of-covariance controlling for age, height, Tanner stage, and gender. The NF1 cohort showed decreased total cross-sectional area [p<0.001], decreased muscle plus bone cross-sectional area [p<0.001], decreased muscle cross-sectional area [p<0.001], and decreased Stress Strain Index [p=0.010]. These data indicate that NF1 individuals have decreased muscle cross-sectional area and decreased bone strength than individuals without NF1.
Asunto(s)
Huesos/fisiopatología , Músculo Esquelético/fisiopatología , Neurofibromatosis 1/fisiopatología , Adolescente , Estudios de Casos y Controles , Niño , Preescolar , Femenino , Humanos , Masculino , Tomografía Computarizada por Rayos XRESUMEN
Wolf-Hirschhorn syndrome (WHS) is a well-known chromosomal disorder attributable to partial deletion of the short arm of chromosome 4 (4p-). Although about 120 cases have been reported so far, there is still very little data on its natural history. Information given to parents at the time of diagnosis tends to be skewed to the extreme negative. To help delineate more thoroughly the natural history of WHS, and to obtain better information to answer parents' questions in a clinical setting, we evaluated 15 patients (12 females, 3 males) in three centers with the 4p- syndrome. Four of the cases had a follow-up spanning 16 years. Thirteen cases were detected by standard cytogenetics (regular G-banding 10, high-resolution banding 3), while the remaining 2 required fluorescence in situ hybridization. A total of 5/15 (33.3%) had heart lesions; 7/15 (46. 6%) had oral facial clefts; 13/15 (86.6%) had a seizure disorder, that tended to disappear with age; and 100% had severe/profound developmental retardation. One Italian patient had sensorineural deafness and 1 Utah patient had a right split hand defect. Of note, 2 Utah patients were able to walk with support (at 4 and 12 years of age, respectively), whereas 3 Italian patients and 1 Utah patient were able to walk unassisted (at 4, 5, 5 years 9 months, and 7 years of age, respectively). Two of the 3 Italian patients also achieved sphincter control (by day). The 8 patients receiving serial electroencephalogram studies showed fairly distinctive abnormalities, usually outlasting seizures. A slow, but constant progress in development was observed in all cases, during the follow-up period. In conclusion, the combined cases of the three centers represent considerable experience, providing new information on several aspects of this important deletion syndrome.
Asunto(s)
Desarrollo Infantil , Anomalías del Ojo , Microcefalia , Anomalías de la Boca , Adolescente , Niño , Preescolar , Deleción Cromosómica , Cromosomas Humanos Par 4 , Oído Externo/anomalías , Femenino , Humanos , Lactante , Discapacidad Intelectual , Masculino , ConvulsionesRESUMEN
Neurofibromatosis type 1 (NF1) is a pleiotropic autosomal dominant disorder with marked variability of clinical expression. As in other heritable disorders, the mapping and cloning of the gene responsible for NF1 have increased our understanding of the pathogenesis of the condition. In particular, the phenotypic variability and variable expressivity can be studied using molecular techniques. In this article we summarize the current knowledge of genotype/phenotype correlation in NF1 and examine the potential molecular basis for variable expressivity. Am. J. Med. Genet. (Semin. Med. Genet.) 89:7-13, 1999.
Asunto(s)
Neurofibromatosis 1/genética , Mapeo Cromosómico , Genes Dominantes , Humanos , Modelos Genéticos , Neurofibromatosis 1/clasificación , Neurofibromatosis 1/fisiopatologíaRESUMEN
Congenital hypoplastic (Diamond-Blackfan) anemia is a rare macrocytic anemia, generally presenting during infancy or childhood. The condition usually occurs sporadically or in a pattern consistent with autosomal recessive inheritance, although autosomal dominant transmission has been proposed in some kindreds. We report the largest known kindred of congenital hypoplastic anemia, with at least 7 affected individuals over 3 generations, and propose that studies of this kindred may be useful for identifying the mechanism by which their genetic abnormality results in congenital hypoplastic anemia. Erythropoietic investigations on relatives show no inhibitors of erythropoiesis in serum, T-lymphocytes, or macrophages. Their erythroid progenitor cells (CFU-E and BFU-E) were generally quantitatively normal, and were capable of rapid proliferation, as judged by cell-cycle shortening. However, their erythroid progenitors displayed a relative insensitivity to recombinant erythropoietin, and produced relatively few normoblasts per erythroid progenitor cell. We propose that these and subsequent studies may be helpful in selecting candidate genes responsible for the molecular defect in this kindred.
Asunto(s)
Anemia Aplásica/congénito , Anemia Macrocítica/congénito , Adolescente , Adulto , Anemia Aplásica/diagnóstico , Anemia Aplásica/genética , Anemia Macrocítica/diagnóstico , Anemia Macrocítica/genética , Preescolar , Células Precursoras Eritroides/efectos de los fármacos , Células Precursoras Eritroides/patología , Eritropoyesis , Eritropoyetina/farmacología , Femenino , Humanos , Masculino , Linaje , Proteínas Recombinantes/farmacologíaRESUMEN
We report on two children who may represent a novel syndrome consisting of a deficiency of immunoglobulin-bearing B lymphocytes and serum antibody, deficient intrauterine and/or postnatal growth, intracranial calcifications, and acquired pancytopenia. Poor growth, intracranial calcifications, developmental delay, and hematological abnormalities are common manifestations of congenital infection. However, humoral immunodeficiency is not characteristic in these infections, and no infection was found on extensive evaluation. Rare genetic syndromes may mimic intrauterine infections and may also include immunodeficiency. However the children reported here lack important characteristics or share distinctive manifestations not described in these disorders. Infants presenting with apparent congenital infections in whom a specific infectious cause cannot be identified should be followed carefully with immunological evaluations since this disorder may be progressive and considerable morbidity is attributable to hematological and immunological manifestations.
Asunto(s)
Encefalopatías/patología , Inmunodeficiencia Variable Común/patología , Trastornos del Crecimiento/patología , Pancitopenia/patología , Encefalopatías/genética , Calcinosis/genética , Inmunodeficiencia Variable Común/genética , Resultado Fatal , Femenino , Trastornos del Crecimiento/genética , Humanos , Lactante , Masculino , Pancitopenia/genética , SíndromeRESUMEN
Aprosencephaly is a rare, lethal malformation sequence of the central nervous system that has been attributed to a postneuralation encephaloclastic process. We describe autopsy findings consistent with aprosencephaly in 2 fetuses conceived from a consanguineous mating (first cousins). Both showed anencephalic manifestations; however, the crania were intact, with fused sutures. The neuropathologic findings were essentially identical. Each fetus had complete absence of the telecephalon and pyramidal tracts, rudimentary diencephalic and mesencephalic structures, primitive cerebellar hemispheres, posterolateral clusters of primitive neural cells in the medullas suggesting an abnormality of neural migration, a normally-formed spinal cord, and retinal dysplasia within normally-formed globes. In addition, both fetuses manifested a peculiar perivascular mesenchymal proliferation seen only within the central nervous system. The similarity of these cases, coupled with parental consanguinity, suggests a primary malformation in brain development due to the homozygous representation of a mutant allele. We hypothesize that these patients may represent a defect in a gene important in brain development, the nature of which has yet to be elucidated.
Asunto(s)
Enfermedades Cerebelosas/congénito , Cerebelo/anomalías , Proteínas de Homeodominio , Prosencéfalo/anomalías , Anomalías Múltiples , Aborto Inducido , Adulto , Enfermedades Cerebelosas/genética , Consanguinidad , Femenino , Feto/anomalías , Feto/patología , Cabeza/anomalías , Humanos , Masculino , Mutación , Proteínas del Tejido Nervioso/genética , Factores de Transcripción Otx , Linaje , Embarazo , Transactivadores/genéticaRESUMEN
Five percent of individuals with neurofibromatosis type 1 (NF1) present with congenital long bone pseudarthrosis (PA). In large series, 50-80% of patients with congenital long bone PA also have NF1. Very little information exists on the natural history and pathogenesis of PA in NF1. This report is a descriptive analysis of a large series of patients with NF1 and tibial bowing or PA. Study A is a case-control study using the National Neurofibromatosis Foundation International Database (NNFFID). Eighty-five patients with PA were compared to a control group from the same database. There was a statistically significant male predominance of NF1 cases with PA (54 males to 31 females), compared to controls (85 males to 87 females) (chi2 = 4.0, P = 0.046, using a two-tailed test with Yates' correction). There was no significant difference in the clinical presentation of NF1 manifestations in NF1 patients with PA than in NF1 patients without PA. Of the affected individuals with PA, there were 24 de novo cases and 21 familial cases (9 through maternal and 12 through paternal inheritance). Questions that could not be answered by Study A were addressed by a partially overlapping case-series report, Study B, in which data on 75 cases ascertained through questionnaires completed by NF center directors were collected. From Study B we determined that half of the patients who had a fracture sustained it before age 2, and approximately 16% of the pseudarthrosis patients had an amputation. Our data indicate a male predominance and no parent-of-origin effect. Male gender may be a susceptibility factor for pseudarthrosis in NF1.
Asunto(s)
Neurofibromatosis 1/complicaciones , Seudoartrosis/etiología , Fracturas de la Tibia/etiología , Adolescente , Adulto , Enfermedades del Desarrollo Óseo/etiología , Estudios de Casos y Controles , Niño , Preescolar , Bases de Datos Factuales , Susceptibilidad a Enfermedades , Femenino , Humanos , Lactante , Masculino , Seudoartrosis/epidemiología , Encuestas y Cuestionarios , Fracturas de la Tibia/epidemiologíaRESUMEN
We describe clinical, pathological and radiological findings in 15 cases of sporadic and familial lower spine agenesis with additional anomalies of the axial skeleton and internal organs and speculate about the cause and pathogenesis of this malformation complex. We show that all of these findings are defects of blastogenesis, originate in the primary developmental field and/or the progenitor fields, thus representing polytopic field defects. This concept appears applicable in our cases and makes such terms such as "caudal regression syndrome" or "axial mesodermal dysplasia spectrum" redundant.
Asunto(s)
Anomalías Múltiples , Vértebras Lumbares/anomalías , Anomalías Múltiples/diagnóstico por imagen , Anomalías Múltiples/embriología , Anomalías Múltiples/mortalidad , Adulto , Consanguinidad , Resultado Fatal , Femenino , Feto/anomalías , Feto/diagnóstico por imagen , Edad Gestacional , Humanos , Lactante , Recién Nacido , Vértebras Lumbares/diagnóstico por imagen , Vértebras Lumbares/embriología , Masculino , Radiografía , SíndromeRESUMEN
Absence of the telencephalon and diencephalon characterizes the syndrome of aprosencephaly, while in atelencephaly, only the telencephalon is absent. Atelencephalic aprosencephaly is characterized by the presence of at least a rudimentary diencephalon. Embryologically, aprosencephaly is thought to occur after the optic vesicles form but before the cerebral vesicles appear. The syndrome is quite rare, with only 10 cases previously reported. We describe two fetuses with atelencephalic aprosencephaly. A 25-week estimated gestational age fetus was born to first-cousin parents and had a prenatal ultrasonographic diagnosis of anencephaly. The second, a 19-week estimated gestational age fetus, was thought to have semilobar holoprosencephaly by prenatal ultrasound. At autopsy, neuropathologic examination in both cases showed virtual absence of the cerebral hemispheres with an incomplete diencephalon. Microscopic examination in one case revealed disorganized neuropil with a proliferative vasculopathy. The optic globes were completely formed and attached to hypoplastic optic nerves, but retinal dysplasia was apparent histologically in both cases, and bilateral colobomata were present in one case. The findings in these cases demonstrate a spectrum of congenital variations that lie between the syndromes of atelencephaly and aprosencephaly, underscoring the complexity of the congenital anomalies.
Asunto(s)
Prosencéfalo/anomalías , Telencéfalo/anomalías , Anomalías Múltiples/diagnóstico por imagen , Anomalías Múltiples/genética , Anomalías Múltiples/patología , Aborto Eugénico , Encéfalo/patología , Consanguinidad , Femenino , Muerte Fetal/patología , Humanos , Recién Nacido , Masculino , Microcefalia/diagnóstico por imagen , Microcefalia/genética , Microcefalia/patología , Embarazo , Prosencéfalo/patología , Síndrome , Telencéfalo/patología , Ultrasonografía PrenatalRESUMEN
The Wolf-Hirschhorn syndrome (WHS) is a well known chromosomal disorder, due to a deletion of distal chromosome 4p. The classical gestalt is striking and poses few diagnostic problems. However, due to the difficulty of detecting very small deletions by standard cytogenetics, diagnosis can be sometimes very difficult, particularly in older patients. In this paper we show the changes, occurring over time, in facial appearance of affected individuals, to improve insight into the evolution of the phenotype, and to increase its diagnostic potential.
Asunto(s)
Anomalías Múltiples/genética , Envejecimiento/patología , Deleción Cromosómica , Cromosomas Humanos Par 4 , Facies , Humanos , Lactante , SíndromeAsunto(s)
Hormonas Estimuladoras de los Melanocitos/farmacología , Melanoma/metabolismo , Proteínas de Neoplasias/biosíntesis , ARN Neoplásico/biosíntesis , Animales , Antineoplásicos/farmacología , Bucladesina/farmacología , Células Cultivadas , AMP Cíclico/metabolismo , Melanoma/ultraestructura , Ratones , Monofenol Monooxigenasa/biosíntesis , Neoplasias Experimentales/metabolismo , Neoplasias Experimentales/ultraestructura , Teofilina/farmacologíaRESUMEN
Neurofibromatosis-Noonan syndrome (NFNS) has been described as a unique phenotype, combining manifestations of neurofibromatosis type 1 (NF1) and Noonan syndrome, which are separate syndromes. Potential etiologies of NFNS include a discrete syndrome of distinct etiology, co-segregation of two mutated common genes, variable clinical expressivity of NF1, and/or allelic heterogeneity. We present an informative family with an unusual NF1 mutation with variable features of NF1 and Noonan syndrome. We hypothesize that an NF1 mutant allele can lead to diagnostic manifestations of Noonan syndrome, supporting the hypothesis that NF1 allelic heterogeneity causes NFNS.
Asunto(s)
Neurofibromatosis 1/complicaciones , Neurofibromatosis 1/genética , Síndrome de Noonan/complicaciones , Síndrome de Noonan/genética , Adolescente , Alelos , Niño , Preescolar , Femenino , Genes de Neurofibromatosis 1 , Humanos , Lactante , Péptidos y Proteínas de Señalización Intracelular/genética , Masculino , Mutación , Linaje , Fenotipo , Proteína Tirosina Fosfatasa no Receptora Tipo 1 , Proteína Tirosina Fosfatasa no Receptora Tipo 11 , Proteínas Tirosina Fosfatasas/genética , Eliminación de SecuenciaRESUMEN
The recent advances in recombinant DNA technology are now being applied to map and clone the genes for dysmorphic syndromes. The genes for almost 40% of the malformation and dysplasia syndromes listed in Smith's Recognizable Patterns of Human Malformation [Jones, 1988] have now been mapped and/or identified. This strategy has dramatically changed the way in which clinical geneticists look at the basic mechanisms of genetic disorders. The primary purpose of applying positional cloning to human disease, including malformation syndromes, is to use the cloned gene to understand the basic pathogenesis of the disorder at hand. The importance of the application of knowledge of mouse models, to human molecular biology and the significance of the role of the clinician in documenting astute observations that assist in mapping cannot be overemphasized. Many of the successful outcomes in gene cloning in dysmorphic syndromes that have occurred thus far were clearly helped by the recognition of patients with chromosomal rearrangements. Collaboration of molecular biologists and clinical geneticists will clearly lead to the continued elucidation of the map location and cloned gene of many other disorders.
Asunto(s)
Mapeo Cromosómico , Cromosomas Humanos/genética , Anomalías Congénitas/genética , Animales , Clonación Molecular , Femenino , Humanos , Masculino , Ratones , SíndromeRESUMEN
In clonogenic assays of hematopoietic progenitors, high concentrations (4 U/mL) of erythropoietin (epo) reduced the formation of granulocyte-macrophage (GM) colonies and diminished the number of granulocytes formed per culture plate. Fetal progenitors were more sensitive to these effects of epo than were progenitors from adults, displaying these reductions at greater than or equal to 1 U epo/mL. The mechanism was investigated by growing fetal progenitors stimulated by recombinant GM-CSF, in the absence of epo, and when eight-cell clones first appeared, mapping their location, then adding epo, and assessing its effect on the subsequent differentiation of the clones. In the absence of epo, the clones developed exclusively into GM colonies. However, if developing clones were presented with epo, 85% matured into GM colonies, but 15% became multilineage or normoblast colonies. In addition, developing clones that were presented with epo produced colonies that contained fewer neutrophils. These effects of epo on neutrophil generation were observed with each of three varieties of recombinant epo, and also with purified human epo, but were not observed using epo that had been neutralized with rabbit anti-epo antiserum.
Asunto(s)
Eritropoyetina/farmacología , Hematopoyesis/efectos de los fármacos , Células Madre Hematopoyéticas/fisiología , Neutrófilos/fisiología , Adulto , Diferenciación Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Ensayo de Unidades Formadoras de Colonias , Factores Estimulantes de Colonias/farmacología , Feto , Factor Estimulante de Colonias de Granulocitos y Macrófagos , Granulocitos/fisiología , Sustancias de Crecimiento/farmacología , Humanos , Recuento de Leucocitos/efectos de los fármacos , Timidina/metabolismo , TritioRESUMEN
Complementary DNAs to rat ventral prostate poly(A) RNA were cloned into pBR322 by the "dG-dC tailing" procedure. Clones containing cDNAs to the mRNAs coding for each of the three subunits of a major secretory protein (prostatein) were identified by hybrid-arrested translation. A 457-nucleotide base pair cDNA (E45) and a portion of a 365-base pair cDNA (E85) were analyzed to determine the composite complete DNA coding sequence for the Mr = 14,000 (C3) subunit of prostatein. A sequence of 12-nucleotide bases (TTTGCTGCTATG) in the signal peptide of C3 was noted to be homologous to signal peptide nucleotide sequences reported in cDNAs coding for the other two prostatein subunits, Mr = 6,000 (C1) and 10,000 (C2). Complementary DNA coding for the C3 subunit was used as a hybridization probe to screen an EcoRI rat genomic DNA library. Two unique 12-kilobase genomic clones, each containing mRNA coding sequences within 2.5-3-kilobase fragments, were identified by restriction enzyme mapping and Southern blot analysis. Restriction enzyme sites within the coding regions of both genes were analogous to the cDNA. Differences in restriction enzyme sites in regions of intervening sequences and flanking DNA established the uniqueness of the two genes. It is suggested that both genes may be transcribed in vivo.
Asunto(s)
Proteína de Unión a Andrógenos/genética , Proteínas Portadoras/genética , ADN/aislamiento & purificación , Genes , Secuencia de Aminoácidos , Proteína de Unión a Andrógenos/aislamiento & purificación , Animales , Secuencia de Bases , Clonación Molecular , Enzimas de Restricción del ADN , Sustancias Macromoleculares , Masculino , Peso Molecular , Poli A/genética , Próstata/metabolismo , Prostateína , ARN/genética , ARN Mensajero/genética , Ratas , Ratas Endogámicas , Secretoglobinas , UteroglobinaRESUMEN
Nuclear and cytosolic forms of a 20-kdalton rat ventral prostate protein were purified and partially sequenced from their N-termini. Isolated nuclei were treated with micrococcal nuclease and extracted in 0.6 M NaCl, and proteins were separated by affinity chromatography on Matrex gel green A, ammonium sulfate fractionation, and fast protein liquid chromatography on Superose 12. The 43 amino acid N-terminal sequence of the nuclear 20-kdalton protein was identical with the cytosolic protein except it lacked 7 N-terminal amino acids present in the cytosolic form. The DNA sequence of a full-length complementary DNA clone isolated from a ventral prostate gt11 library extended the N-terminal sequence of the cytosolic form by an additional nine amino acids from the predicted initiation methionine. The cDNA included the nucleotide sequence for the 43 amino acid N-terminal sequence of the purified 20-kdalton protein and predicted molecular weights of 16,686, 17,521, and 18,650, respectively, for the nuclear, cytoplasmic, and nonprocessed proteins. Northern blot analyses of reproductive tract tissue RNAs using the 20-kdalton protein cDNA as probe revealed a single mRNA species of 0.92 kb detectable only in extracts of rat ventral prostate. Expression of the 0.92-kb mRNA was androgen dependent since the mRNA was undetectable in extracts obtained 4 days after castration and was restored 16 h after restimulation with androgen.