دورية أكاديمية

ORIGINAL ARTICLE Regulation of pri-microRNA BIC transcription and processing in

التفاصيل البيبلوغرافية
العنوان: ORIGINAL ARTICLE Regulation of pri-microRNA BIC transcription and processing in
المؤلفون: Burkitt Lymphoma, J Kluiver, A Van Den Berg, D De Jong, T Blokzijl, G Harms, E Bouwman, S Jacobs, B-j Kroesen
المساهمون: The Pennsylvania State University CiteSeerX Archives
المصدر: http://www.rug.nl/research/pathology/medbiol/pdf/kluiver-kroesen_oncogene_06.pdfTest.
المجموعة: CiteSeerX
مصطلحات موضوعية: BIC, microRNA-155, Burkitt lymphoma, microRNA processing, B-cell receptor
الوصف: BIC is a primary microRNA (pri-miR-155) that can be processed to mature miR-155. In this study, we show the crucial involvement of protein kinase C (PKC) and nuclear factor-jB (NF-jB) in the regulation of BIC expression upon B-cell receptor triggering. Surprisingly, Northern blot analysis did not reveal any miR-155 expression upon induction of BIC expression in the Burkitt lymphoma-derived Ramos cell line, whereas other microRNAs were clearly detectable. Ectopic expression of BIC in Ramos and HEK293 cells resulted in miR-155 expression in HEK293, but not in Ramos cells, suggesting a specific block of BIC to miR-155 processing in Ramos. In line with the results obtained with Ramos, lack of miR-155 expression after induction of BIC expression was also observed in other Burkitt lymphoma cell lines, indicating a generic and specific blockade in the processing of BIC in Burkitt lymphoma. In contrast, induction of BIC expression in normal tonsillar B cells resulted in very high levels of miR-155 expression and induction of BIC expression in Hodgkin’s lymphoma cell lines. It also resulted in elevated levels of miR-155. Our data provide evidence for two levels of regulation for mature miR-155 expression: one at the transcriptional level involving PKC and NF-jB, and one at the processing level. Burkitt lymphoma cells not only express low levels of BIC, but also prevent processing of BIC via an, as yet, unknown mechanism. Oncogene advance online publication, 18 December 2006; doi:10.1038/sj.onc.1210147
نوع الوثيقة: text
وصف الملف: application/pdf
اللغة: English
العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.333.9800Test; http://www.rug.nl/research/pathology/medbiol/pdf/kluiver-kroesen_oncogene_06.pdfTest
الإتاحة: http://www.rug.nl/research/pathology/medbiol/pdf/kluiver-kroesen_oncogene_06.pdfTest
حقوق: Metadata may be used without restrictions as long as the oai identifier remains attached to it.
رقم الانضمام: edsbas.E5AC9904
قاعدة البيانات: BASE