A subclass of Ras proteins that regulate the degradation of IκB

被引:87
作者
Fenwick, C
Na, SY
Voll, RE
Zhong, HH
Im, SY
Lee, JW
Ghosh, S [1 ]
机构
[1] Chonnam Natl Univ, Ctr Ligand & Transcript, Kwangju 500757, South Korea
[2] Yale Univ, Sch Med, Howard Hughes Med Inst, Immunobiol Sect, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Howard Hughes Med Inst, Dept Mol Biophys & Biochem, New Haven, CT 06510 USA
[4] Chonnam Natl Univ, Dept Biol, Kwangju 500757, South Korea
[5] Chonnam Natl Univ, Dept Microbiol, Kwangju 500757, South Korea
[6] Chonnam Natl Univ, Hormone Res Ctr, Kwangju 500757, South Korea
关键词
D O I
10.1126/science.287.5454.869
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Small guanosine triphosphatases, typified by the mammalian Ras proteins, play major roles in the regulation of numerous cellular pathways. A subclass of evolutionarily conserved Ras-Like proteins was identified, members of which differ from other Ras proteins in containing amino acids at positions 12 and 61 that are similar to those present in the oncogenic forms of Ras. These proteins, kappa B-Ras1 and kappa B-Ras2, interact with the PEST domains of I kappa B alpha and I kappa B beta [inhibitors of the transcription factor nuclear factor kappa B (NF-kappa B)] and decrease their rate of degradation. In cells, kappa B-Ras proteins are associated only with NF-kappa B:I kappa B beta complexes and therefore may provide an explanation for the slower rate of degradation of I kappa B beta compared with I kappa B alpha.
引用
收藏
页码:869 / 873
页数:5
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