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1.
Microb Pathog ; 47(3): 183-7, 2009 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-19555754

RESUMEN

We have previously reported that some pseudogenes are expressed in Mycobacterium leprae (M. leprae), the causative agent of leprosy, and that their expression levels alter upon infection of macrophages. We attempted to further examine the expression of pseudogene and non-coding genomic region in M. leprae, in this study. 19 Pseudogenes, 17 non-coding genomic regions, and 21 coding genes expression in M. leprae maintained in the footpads of the hypertensive nude rat (SHR/NCrj-rnu) were examined by reverse transcriptase polymerase chain reaction (RT-PCR). The expression of some of these pseudogenes, non-coding genomic regions and coding genes were also examined in M. leprae from skin smear specimens obtained from patients with lepromatous leprosy by RT-PCR. Transcripts from pseudogenes, non-coding genomic regions and coding genes examined in this study were clearly observed in M. leprae. The expression patterns of some of these transcripts vary greatly among different leprosy patients. These results indicate that some of pseudogenes and non-coding genomic regions are transcribed in M. leprae and analysis of RNA expression patterns including pseudogene and non-coding genomic region in M. leprae may be useful in understanding the pathological states of infected patients.


Asunto(s)
Genoma Bacteriano , Lepra/microbiología , Mycobacterium leprae/genética , Seudogenes , ARN no Traducido/genética , Animales , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Regulación Bacteriana de la Expresión Génica , Humanos , Mycobacterium leprae/metabolismo , ARN Bacteriano/genética , Ratas , Ratas Desnudas
2.
Nihon Hansenbyo Gakkai Zasshi ; 78(1): 49-54, 2009 Feb.
Artículo en Japonés | MEDLINE | ID: mdl-19227149

RESUMEN

Completion of Mycobacterium leprae genome sequence revealed that there are many pseudogenes and non-coding regions, but rather small numbers of protein-coding genes. Although it was thought that pseudogenes and non-coding regions were silent and junk, our previous studies indicated that RNA expression was detected from these regions. To elucidate comprehensive RNA expression pattern on M. leprae whole genome, tiling array was designed and total RNA of M. leprae Thai-53 strain was analyzed. As a result, highly expressed regions were detected among not only the gene regions but also pseudogenes and non-coding regions. Since some of the RNA expression levels were modulated by MDT, evaluation of RNA expression pattern might be a good indicator for the treatment of leprosy.


Asunto(s)
Expresión Génica , Genoma Bacteriano/genética , Mycobacterium leprae/genética , Análisis de Secuencia por Matrices de Oligonucleótidos/métodos , ARN Bacteriano/genética , Seudogenes/genética
3.
Nihon Hansenbyo Gakkai Zasshi ; 78(1): 61-5, 2009 Feb.
Artículo en Japonés | MEDLINE | ID: mdl-19227151

RESUMEN

Completion of Mycobacterium leprae genome sequence revealed that there are many pseudogenes and non-coding regions, but rather small numbers of protein-coding genes. This result indicates that M. leprae is a very unique organism, and this future is important to understand the biological nature and/or pathogenicity of M. leprae, which remain unclear. We attempted to find the biological nature of M. leprae by detecting the gene and pseudogene regions transcribed at high level. We detected the genomic regions including pseudogenes and demonstrated that six out of twelve high expression regions were pseudogenes. In addition, its transcription level was changed when M. leprae infects macrophage. RNA was detected from genes, pseudogenes and non-coding regions. The expression levels of these regions were different among patients and a part of them is disappeared just after treatment. These results suggested that RNA derived from pseudogene and non-coding region have some function concerning the infection and/or intracellular parasitism and that the analysis of pseudogene and non-coding region expression pattern of M. leprae is available as a criterion for therapeutic effect and disease type of leprosy, and a prognostic marker.


Asunto(s)
Expresión Génica/genética , Genoma Bacteriano/genética , Mycobacterium leprae/genética , Humanos , Análisis de Secuencia por Matrices de Oligonucleótidos , Seudogenes/genética , ARN Bacteriano , Transcripción Genética/genética
4.
FEMS Microbiol Lett ; 289(1): 72-9, 2008 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-19054096

RESUMEN

Mycobacterium leprae survives and replicates within a lipid droplet stored in the enlarged phagosome of histiocytes, a typical feature of lepromatous leprosy that is thought to be an important nutrient source for the bacillus. However, the underlying mechanisms by which lipids accumulate within phagosomes remain unclear. Recently, it was revealed that the lipid droplet-associated proteins, including ADRP and perilipin, play essential roles in lipid accumulation in adipocytes or macrophages. Therefore, we attempted to examine the role of these proteins in leprosy pathogenesis. ADRP and perilipin localized to the phagosomal membrane, which contains M. leprae in skin biopsy specimens of lepromatous leprosy. ADRP expression was transiently increased after phagocytosis in THP-1 cells. However, high levels of ADRP expression persisted only when live M. leprae, but not dead bacilli or latex beads, was added. Furthermore, although peptidoglycan, a Toll-like receptor 2 ligand, suppressed the expression levels of ADRP and perilipin, M. leprae infection inhibited this suppression. These results suggest that live M. leprae has the ability to actively induce and support ADRP/perilipin expression to facilitate the accumulation of lipids within the phagosome and to further maintain a suitable environment for the intracellular survival within the macrophage.


Asunto(s)
Regulación de la Expresión Génica , Lepra Lepromatosa/metabolismo , Macrófagos/microbiología , Proteínas de la Membrana/metabolismo , Mycobacterium leprae/patogenicidad , Fosfoproteínas/metabolismo , Animales , Proteínas Portadoras , Línea Celular , Humanos , Lepra Lepromatosa/patología , Macrófagos/metabolismo , Proteínas de la Membrana/genética , Ratones , Ratones Desnudos , Perilipina-1 , Perilipina-2 , Fosfoproteínas/genética , ARN Mensajero/genética , ARN Mensajero/metabolismo , Piel/metabolismo , Piel/microbiología , Piel/patología
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