NF-κB binds P-TEFb to stimulate transcriptional elongation by RNA polymerase II

被引:379
|
作者
Barboric, M
Nissen, RM
Kanazawa, S
Jabrane-Ferrat, N
Peterlin, BM [1 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Med, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Microbiol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Immunol, San Francisco, CA 94143 USA
[4] MIT, Canc Res Ctr, Cambridge, MA 02139 USA
[5] Univ Ljubljana, Fac Med, Inst Biochem, Ljubljana 1000, Slovenia
关键词
D O I
10.1016/S1097-2765(01)00314-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To stimulate transcriptional elongation of HIV-1 genes, the transactivator Tat recruits the positive transcription elongation factor b (P-TEFb) to the initiating RNA polymerase II (RNAPII). We found that the activation of transcription by ReIA also depends on P-TEFb. Similar to Tat, ReIA activated transcription when tethered to RNA. Moreover, TNF-alpha triggered the recruitment of P-TEFb to the NF-B-K-regulated IL-8 gene. While the formation of the transcription preinitiation complex (PIC) remained unaffected, DRB, an inhibitor of P-TEFb, prevented RNAPII from elongating on the IL-8 gene. Remarkably, DRB inhibition sensitized cells to TNF-alpha -induced apoptosis. Thus, NF-B-K requires P-TEFb to stimulate the elongation of transcription and P-TEFb plays an unexpected role in regulating apoptosis.
引用
收藏
页码:327 / 337
页数:11
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