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2.
J Cardiovasc Transl Res ; 16(1): 77-85, 2023 02.
Artículo en Inglés | MEDLINE | ID: mdl-35759180

RESUMEN

Myocardial fibrosis confers an almost threefold mortality risk in heart disease. There are no prognostic therapies and novel therapeutic targets are needed. Many thousands of unannotated small open reading frames (smORFs) have been identified across the genome with potential to produce micropeptides (< 100 amino acids). We sought to investigate the role of smORFs in myocardial fibroblast activation.Analysis of human cardiac atrial fibroblasts (HCFs) stimulated with profibrotic TGFß1 using RNA sequencing (RNA-Seq) and ribosome profiling (Ribo-Seq) identified long intergenic non-coding RNA LINC01013 as TGFß1 responsive and containing an actively translated smORF. Knockdown of LINC01013 using siRNA reduced expression of profibrotic markers at baseline and blunted their response to TGFß1. In contrast, overexpression of a codon-optimised smORF invoked a profibrotic response comparable to that seen with TGFß1 treatment, whilst FLAG-tagged peptide associated with the mitochondria.Together, these data support a novel LINC01013 smORF micropeptide-mediated mechanism of fibroblast activation. TGFß1 stimulation of atrial fibroblasts induces expression of LINC01013, whose knockdown reduces fibroblast activation. Overexpression of a smORF contained within LINC01013 localises to mitochondria and activates fibroblasts.


Asunto(s)
Fibrilación Atrial , ARN Largo no Codificante , Humanos , Proteómica , ARN Largo no Codificante/genética , Fibroblastos , Micropéptidos
3.
Mol Psychiatry ; 17(12): 1328-39, 2012 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21968932

RESUMEN

In a previous study, we detected a 6p25-p24 region linked to schizophrenia in families with high composite cognitive deficit (CD) scores, a quantitative trait integrating multiple cognitive measures. Association mapping of a 10 Mb interval identified a 260 kb region with a cluster of single-nucleotide polymorphisms (SNPs) significantly associated with CD scores and memory performance. The region contains two colocalising genes, LYRM4 and FARS2, both encoding mitochondrial proteins. The two tagging SNPs with strongest evidence of association were located around the overlapping putative promoters, with rs2224391 predicted to alter a transcription factor binding site (TFBS). Sequencing the promoter region identified 22 SNPs, many predicted to affect TFBSs, in a tight linkage disequilibrium block. Luciferase reporter assays confirmed promoter activity in the predicted promoter region, and demonstrated marked downregulation of expression in the LYRM4 direction under the haplotype comprising the minor alleles of promoter SNPs, which however is not driven by rs2224391. Experimental evidence from LYRM4 expression in lymphoblasts, gel-shift assays and modelling of DNA breathing dynamics pointed to two adjacent promoter SNPs, rs7752203-rs4141761, as the functional variants affecting expression. Their C-G alleles were associated with higher transcriptional activity and preferential binding of nuclear proteins, whereas the G-A combination had opposite effects and was associated with poor memory and high CD scores. LYRM4 is a eukaryote-specific component of the mitochondrial biogenesis of Fe-S clusters, essential cofactors in multiple processes, including oxidative phosphorylation. LYRM4 downregulation may be one of the mechanisms involved in inefficient oxidative phosphorylation and oxidative stress, increasingly recognised as contributors to schizophrenia pathogenesis.


Asunto(s)
Trastornos del Conocimiento/genética , Genes Sobrepuestos/genética , Proteínas Reguladoras del Hierro/genética , Proteínas Mitocondriales/genética , Regiones Promotoras Genéticas/genética , Esquizofrenia/genética , Psicología del Esquizofrénico , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Alelos , Estudios de Casos y Controles , Línea Celular , Trastornos del Conocimiento/complicaciones , Femenino , Expresión Génica/genética , Estudios de Asociación Genética/estadística & datos numéricos , Humanos , Proteínas Reguladoras del Hierro/metabolismo , Masculino , Persona de Mediana Edad , Proteínas Mitocondriales/metabolismo , Fenilalanina-ARNt Ligasa/genética , Polimorfismo de Nucleótido Simple/genética , Esquizofrenia/complicaciones
6.
Biochem Soc Trans ; 34(Pt 2): 328-9, 2006 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-16545106

RESUMEN

We describe cellular engineering for the creation of multiple new cellular modules each composed of an orthogonal ribosome and orthogonal mRNA. These modules operate independently of the endogenous ribosome and mRNA. We discuss some of the applications of orthogonal pairs and highlight the expression of Boolean logic in gene regulation using multiple orthogonal pairs.


Asunto(s)
Evolución Biológica , ARN Mensajero/metabolismo , Ribosomas/metabolismo , Regulación de la Expresión Génica , Unión Proteica , Biosíntesis de Proteínas , ARN Mensajero/química , ARN Mensajero/genética , Ribosomas/química
7.
Arch Dis Child ; 87(2): 147-8, 2002 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-12138068

RESUMEN

Retrospective review of serum immunoglobulin levels in 78 methotrexate treated paediatric rheumatology patients showed that IgG, IgA, and IgM levels fell significantly by 26%, 21%, and 17% respectively while on methotrexate. Six patients with systemic disease showed a fall in IgG to below the normal range.


Asunto(s)
Antirreumáticos/farmacología , Artritis Juvenil/tratamiento farmacológico , Inmunoglobulinas/efectos de los fármacos , Inmunosupresores/farmacología , Metotrexato/farmacología , Antirreumáticos/uso terapéutico , Artritis Juvenil/inmunología , Niño , Humanos , Inmunoglobulina G/sangre , Inmunoglobulina G/efectos de los fármacos , Inmunoglobulinas/sangre , Inmunosupresores/uso terapéutico , Metotrexato/uso terapéutico , Estudios Retrospectivos
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