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1.
Physiol Genomics ; 50(9): 680-687, 2018 09 01.
Article in English | MEDLINE | ID: mdl-29775428

ABSTRACT

Hypertrophic cardiomyopathy thickens heart muscles, reducing functionality and increasing risk of cardiac disease and morbidity. Genetic factors are involved, but their contribution is poorly understood. We used the hypertrophic heart rat (HHR), a unique normotensive polygenic model of cardiac hypertrophy and heart failure, to investigate the role of genes associated with monogenic human cardiomyopathy. We selected 42 genes involved in monogenic human cardiomyopathies to study: 1) DNA variants, by sequencing the whole genome of 13-wk-old HHR and age-matched normal heart rat (NHR), its genetic control strain; 2) mRNA expression, by targeted RNA-sequencing in left ventricles of HHR and NHR at 5 ages (2 days old and 4, 13, 33, and 50 wk old) compared with human idiopathic dilated cardiomyopathy data; and 3) microRNA expression, with rat microRNA microarrays in left ventricles of 2-day-old HHR and age-matched NHR. We also investigated experimentally validated microRNA-mRNA interactions. Whole-genome sequencing revealed unique variants mostly located in noncoding regions of HHR and NHR. We found 29 genes differentially expressed in at least 1 age. Genes encoding desmoglein 2 ( Dsg2) and transthyretin ( Ttr) were significantly differentially expressed at all ages in the HHR, but only Ttr was also differentially expressed in human idiopathic cardiomyopathy. Lastly, only two microRNAs differentially expressed in the HHR were present in our comparison of validated microRNA-mRNA interactions. These two microRNAs interact with five of the genes studied. Our study shows that genes involved in monogenic forms of human cardiomyopathies may also influence polygenic forms of the disease.


Subject(s)
Cardiomegaly/genetics , Cardiomyopathies/genetics , Multifactorial Inheritance/genetics , Animals , Binding Sites , Gene Expression Profiling , Gene Expression Regulation , Genome-Wide Association Study , Humans , Myocardium/metabolism , Myocardium/pathology , Polymorphism, Single Nucleotide/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats , Sequence Analysis, DNA
3.
Ann Hum Genet ; 72(Pt 1): 57-64, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17683516

ABSTRACT

BACKGROUND: Machado-Joseph disease (MJD SCA3), a spinocerebellar ataxia related to expansion of a CAG tract, has already been related to anticipation and meiotic drift. However, fitness of MJD carriers has been little studied. OBJECTIVE: To analyze genetic fitness of MJD patients, comparing them to their unaffected relatives and to the general population (GP) of origin. SUBJECTS AND METHODS: 182 informants, belonging to 82 MJD families, agreed to participate in the study. Informants supplied data about 828 MJD patients. Number of children (NC), gender, age, school attainment, menarche and menopause were compared between general and emeritus (older than 45 years of age or deceased) groups. RESULTS: Mean NC of the GP and of MJD patients were respectively 1.90 and 2.93+/-2.3 (p = 0.0037). Comparisons within families also showed differences: the mean NC of unaffected and affected emeritus MJD women were, respectively, 2.68 and 3.89 (p = 0.0037). Affected MJD women had earlier mean ages at the delivery of their first child and menopause (p < 0.011 and 0.07, respectively). Among affected women those who did not have children had larger CAG tracts than those who had children (p < 0.05). CONCLUSION: MJD enhances the fitness of its carriers, and this phenomenon seems to have a biological basis.


Subject(s)
Machado-Joseph Disease/genetics , Population Groups , Age of Onset , Brazil/epidemiology , Case-Control Studies , Child , Cohort Studies , Female , Heterozygote , Humans , Machado-Joseph Disease/epidemiology , Machado-Joseph Disease/pathology , Prevalence
4.
Clin Genet ; 72(6): 543-5, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17894834

ABSTRACT

Machado-Joseph disease (MJD), one of the most prevalent autosomal dominant cerebellar ataxias, is a neurodegenerative disease that starts during adulthood, with patients showing difficulties in gait, later becoming bedridden, and ultimately presenting premature death. There is, however, scarce data quantifying disease impact on patient survival. We investigated the overall survival of a large series of MJD patients and compared it with the survival of their asymptomatic relatives. A total of 412 affected and 413 unaffected individuals were ascertained from a consecutive sample of 82 families with a molecular diagnosis of MJD. Estimated mean survival time was 63.96 years [95% confidence interval (CI), 62.09-65.83] for the affected group and 78.61 years (95% CI, 74.75-82.47) for the unaffected group (p < 0.001). For a subset of 366 patients, mean age at onset was 36.37 years (95% CI, 35.21-37.53) and survival after disease onset was estimated as 21.18 years. Early onset and large CAG length predicted shorter overall survival times. This study presents quantitative data on the impact of MJD on overall survival, a phenomenon that is related to CAG length, age at onset, and year of birth.


Subject(s)
Machado-Joseph Disease/genetics , Machado-Joseph Disease/mortality , Adolescent , Adult , Age of Onset , Aged , Ataxin-3 , Child , Female , Humans , Male , Middle Aged , Nerve Tissue Proteins/genetics , Nuclear Proteins/genetics , Repressor Proteins/genetics , Survival Rate , Trinucleotide Repeat Expansion
5.
Arch Insect Biochem Physiol ; 62(4): 176-85, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16933279

ABSTRACT

Ornithine decarboxylase (ODC) activity was analyzed in Anastrepha fraterculus (Diptera) females (4 days old) submitted to temperature stress (6 degrees C and 20/6 degrees C) and the topical application of juvenile hormone (JH). ODC activity and ejaculatory apodeme measurements (length and width) were made in males (15 days old) after 6 degrees C stress. JH dose of 500 ng and incubation of 3, 7, and 18 h increased ODC activity. Females reared at 6 degrees C and 20/6 degrees C had higher ODC activity than those reared at 25 degrees C. The treatment of 6 degrees C and JH incubation for 1 h increased ODC activity when compared to 6 degrees C treatments only. However, the treatment of 20/6 degrees C only after 3 or 18 h of JH incubation resulted in higher ODC activity than controls (20/6 degrees C) or 20/6 degrees C plus 1 h of JH incubation. Males did not undergo differences in ODC activity when reared at 6 degrees C or 25 degrees C but the ejaculatory apodeme measurements was higher in those reared at 25 degrees C than in those reared at 6 degrees C. The results can be considered an adaptive process to environmental changes.


Subject(s)
Juvenile Hormones/pharmacology , Ornithine Decarboxylase/metabolism , Temperature , Tephritidae/enzymology , Administration, Topical , Analysis of Variance , Animals , Enzyme Activation/drug effects , Female , Genitalia, Male/drug effects , Juvenile Hormones/administration & dosage , Male , Tephritidae/drug effects , Time Factors
6.
Arch Insect Biochem Physiol ; 57(4): 151-9, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15540277

ABSTRACT

Ornithine decarboxylase (ODC) (EC 4.1.1.17) is very important for polyamine biosynthesis, which is required for main biological events. In the present study, ODC activity was measured in samples of Anastrepha fraterculus's egg, larva, pupa body and abdomen, adult body, ovaries, and fat body of young females, and in ovaries of mature flies. The kinetic parameters (Km app and Vmax) for ODC activity were determined for pupa, larva, and young ovary. ODC activity showed fluctuations during A. fraterculus's life development. In its earlier stages, prior to emergence, the egg has high ODC-specific activity probably due to embryogenesis, which is characterized by a high rate of cell division. This enzyme activity is also significantly high in the ovary and fat body of young females possibly related to the increased oogenesis and vitellogenesis. The kinetic parameters (Km app and Vmax) had great variation. Our results using GTP showed that the great variation in kinetic parameters can be accounted for by post-translational modifications.


Subject(s)
Ornithine Decarboxylase/metabolism , Tephritidae/enzymology , Tephritidae/growth & development , Animals , Dose-Response Relationship, Drug , Enzyme Activation/drug effects , Fat Body/metabolism , Female , Guanosine Triphosphate/pharmacology , Kinetics , Larva/enzymology , Ovary/metabolism , Ovum/metabolism , Pupa/enzymology
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