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Cryo-EM visualization of a viral internal ribosome entry site bound to human ribosomes: The IRES functions as an RNA-Based translation factor
被引:213
作者:
Spahn, CMT
Jan, E
Mulder, A
Grassucci, RA
Sarnow, P
Frank, J
机构:
[1] New York State Dept Hlth, Wadsworth Ctr Labs & Res, Howard Hughes Med Inst, Hlth Res Inc, Albany, NY 12201 USA
[2] SUNY Albany, Dept Biomed Sci, Albany, NY 10012 USA
[3] Charite Univ Med Berlin, Inst Med Phys & Biophys, D-10117 Berlin, Germany
[4] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[5] Purdue Univ, Dept Biol, W Lafayette, IN 47906 USA
来源:
关键词:
D O I:
10.1016/j.cell.2004.08.001
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:
Internal initiation of protein synthesis in eukaryotes is accomplished by recruitment of ribosomes to structured internal ribosome entry sites (IRESs), which are located in certain viral and cellular messenger RNAs. An IRES element in cricket paralysis virus (CrPV) can directly assemble 80S ribosomes in the absence of canonical initiation factors and initiator tRNA. Here we present cryo-EM structures of the CrPV IRES bound to the human ribosomal 40S subunit and to the 80S ribosome. The CrPV IRES adopts a defined, elongate structure within the ribosomal intersubunit space and forms specific contacts with components of the ribosomal A, P, and E sites. Conformational changes in the ribosome as well as within the IRES itself show that CrPV IRES actively manipulates the ribosome. CrPV-Iike IRES elements seem to act as RNA-based translation factors.
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页码:465 / 475
页数:11
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