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免疫球蛋白μ转换区中的两个反义启动子驱动伯基特淋巴瘤细胞系BL67中c-myc的表达。

Two antisense promoters in the immunoglobulin mu-switch region drive expression of c-myc in the Burkitt's lymphoma cell line BL67.

作者信息

Apel T W, Mautner J, Polack A, Bornkamm G W, Eick D

机构信息

Institut für Klinische Molekularbiologie und Tumorgenetik, Forschungszentrum für Umwelt and Gesundheit, GSF, München-Grosshadern, Germany.

出版信息

Oncogene. 1992 Jul;7(7):1267-71.

PMID:1620543
Abstract

In the Burkitt's lymphoma (BL) cell line BL67 the first exon of the c-myc gene is fused to the mu-switch region of the immunoglobulin heavy-chain gene (IgH). BL67 cells express IgH/c-myc hybrid RNAs which are initiated in the immunoglobulin locus, transcribed across the chromosomal breakpoint into the first exon of c-myc and spliced using the physiological splice donor and acceptor sites of the c-myc gene. We have isolated cDNAs of these hybrid RNAs and characterized the start points in the Ig heavy-chain gene. Two promoters were identified in the mu-switch region of BL67 cells which give rise to antisense transcription of the mu-gene. These promoters are also active in other BL cell lines, in B cells without Ig translocation and in a T-cell line. Both promoters co-localize with DNAase I-hypersensitive sites, HNF and HSW, in the mu-switch region. The structures of IgH/c-myc hybrid RNAs and of the corresponding promoters are described.

摘要

在伯基特淋巴瘤(BL)细胞系BL67中,c-myc基因的第一个外显子与免疫球蛋白重链基因(IgH)的μ转换区融合。BL67细胞表达IgH/c-myc杂合RNA,这些RNA在免疫球蛋白基因座起始,转录穿过染色体断点进入c-myc的第一个外显子,并使用c-myc基因的生理剪接供体和受体位点进行剪接。我们已分离出这些杂合RNA的cDNA,并对Ig重链基因中的起始点进行了表征。在BL67细胞的μ转换区鉴定出两个启动子,它们导致μ基因的反义转录。这些启动子在其他BL细胞系、无Ig易位的B细胞和一个T细胞系中也有活性。两个启动子都与μ转换区的DNA酶I超敏位点HNF和HSW共定位。本文描述了IgH/c-myc杂合RNA和相应启动子的结构。

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