RESUMEN
Protein arginine N-methyltransferases have been implicated in a variety of processes, including cell proliferation, signal transduction, and protein trafficking. In this study, we have characterized essentially a null mutation induced by insertion of the U3betaGeo gene trap retrovirus into the second intron of the mouse protein arginine N-methyltransferase 1 gene (Prmt1). cDNAs encoding two forms of Prmt1 were characterized, and the predicted protein sequences were found to be highly conserved among vertebrates. Expression of the Prmt1-betageo fusion gene was greatest along the midline of the neural plate and in the forming head fold from embryonic day 7.5 (E7.5) to E8.5 and in the developing central nervous system from E8.5 to E13.5. Homozygous mutant embryos failed to develop beyond E6.5, a phenotype consistent with a fundamental role in cellular metabolism. However, Prmt1 was not required for cell viability, as the protein was not detected in embryonic stem (ES) cell lines established from mutant blastocysts. Low levels of Prmt1 transcripts (approximately 1% of the wild-type level) were detected as assessed by a quantitative reverse transcription-PCR assay. Total levels of arginine N-methyltransferase activity and asymmetric N(G), N(G)-dimethylarginine were reduced by 85 and 54%, respectively, while levels of hypomethylated substrates were increased 15-fold. Prmt1 appears to be a major type I enzyme in ES cells, and in wild-type cells, most substrates of the enzyme appear to be maintained in a fully methylated state.
Asunto(s)
Desarrollo Embrionario , Desarrollo Embrionario y Fetal , Proteína-Arginina N-Metiltransferasas/genética , Proteína-Arginina N-Metiltransferasas/metabolismo , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Blastocisto/enzimología , Supervivencia Celular/genética , Mapeo Cromosómico , Femenino , Muerte Fetal/genética , Regulación del Desarrollo de la Expresión Génica , Genes Letales , Genes Recesivos , Homocigoto , Metilación , Ratones , Ratones Endogámicos C57BL , Ratones Mutantes , Datos de Secuencia Molecular , Mutación , Embarazo , Provirus/genética , Células Madre/fisiologíaRESUMEN
The Klippel-Trénaunay-Weber (KTW) syndrome is a congenital disorder of angiogenesis characterized by macular nevus, skeletal and soft tissue hypertrophy, venous varicosities, and arteriovenous fistulas. Disseminated intravascular coagulation (DIC) and the Kasabach-Merritt syndrome, a consumptive coagulopathy with thrombocytopenia, are both associated with the KTW syndrome. We describe a 30-year-old woman with KTW syndrome and Kasabach-Merritt syndrome who had DIC with severe hemorrhage after a routine gynecologic procedure. The bleeding was controlled with the use of intravenous low-dose heparin and antithrombin III.
Asunto(s)
Coagulación Intravascular Diseminada/diagnóstico , Electrocirugia , Síndrome de Klippel-Trenaunay-Weber/diagnóstico , Hemorragia Posoperatoria/etiología , Trombocitopenia/diagnóstico , Displasia del Cuello del Útero/cirugía , Adulto , Pruebas de Coagulación Sanguínea , Coagulación Intravascular Diseminada/sangre , Femenino , Humanos , Síndrome de Klippel-Trenaunay-Weber/sangre , Hemorragia Posoperatoria/sangre , Hemorragia Posoperatoria/diagnóstico , Recurrencia , Trombocitopenia/sangre , Displasia del Cuello del Útero/sangreAsunto(s)
Vectores Genéticos , Mutagénesis Insercional , Retroviridae , Células Madre/citología , Animales , Células Cultivadas , Quimera , Células Clonales , Técnicas de Cultivo/métodos , Embrión de Mamíferos , Fibroblastos/citología , Expresión Génica , Humanos , Ratones , Ratones Transgénicos , Fenotipo , Plásmidos , Células Madre/fisiología , Transcripción GenéticaRESUMEN
A challenge design was employed to investigate the effect of sucrose consumption on the behavior of 12 preschool children. On separate experimental days, subjects were tested individually with either a challenge sucrose drink (2 gm/kg body weight) or a placebo drink sweetened with aspartame. Fifteen-minute observations of each child during free play were made at 15, 45, and 75 minutes after ingestion of the drink. Assessment with a paired-associate learning task was made before ingestion and at 30, 60, and 90 minutes after ingestion. This study was a partial replication and extension of one of the few studies in the literature that has found an effect of sucrose on the behavior of normal children. On all dependent measures (locomotion, task orientation, and learning), the study failed to obtain significant differences between the two conditions.