Bistabillity in the JNK cascade

被引:180
作者
Bagowski, CP [1 ]
Ferrell, JE [1 ]
机构
[1] Stanford Univ, Sch Med, Div Chem Biol, Stanford, CA 94305 USA
关键词
D O I
10.1016/S0960-9822(01)00330-X
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
Background: Important signaling properties, like adaptation, oscillations, and bistability, can emerge at the level of relatively simple systems of signaling proteins. Here, we have examined the quantitative properties of one well-studied signaling system, the JNK cascade. We experimentally assessed the response of JNK to a physiological stimulus (progesterone) and a pathological stress (hyperosmolar sorbitol) in Xenopus laevis oocytes, a cell type that is well-suited to the quantitative analysis of cell signaling. Our aim was to determine whether JNK responses are graded (Michaelian) in character; ultrasensitive in character, resembling the responses of cooperative enzymes; or bistable and all-or-none in character. Results: The responses of JNK to both progesterone and sorbitol were found to be essentially all-or-none. Individual oocytes had either very high or very low JNK activities, with few oocytes possessing intermediate levels of JNK activity. Moreover, JNK activation was autocatalytic, indicating that the JNK cascade is either embedded in or downstream of a positive feedback loop. JNK also exhibited hysteresis, a form of biochemical memory, in its response to sorbitol. These findings indicate that the JNK cascade is part of a bistable signaling system in oocytes. Conclusions: In Xenopus oocytes, JNK responds to physiological and pathological stimuli in an all-or-none manner. The JNK response shows all the hallmarks of a bistable response, including strong positive feedback and hysteresis. Bistability is a recurring theme in the biochemistry of oocyte maturation and early embryogenesis; the Mos/MEK/p42 MAPK cascade also exhibits bistable responses, and the Cdc2/cyclin B system is hypothesized to be bistable as well. However, the mechanisms underpinning the positive feedback and bistability in the three cases are different, suggesting that evolution has repeatedly converged upon bistability as a way of producing digital responses.
引用
收藏
页码:1176 / 1182
页数:7
相关论文
共 37 条
[1]  
[Anonymous], BIOCH BIOPHYS ACTA
[2]   c-jun N-terminal kinase activation in Xenopus laevis eggs and embryos -: A possible non-genomic role for the JNK signaling pathway [J].
Bagowski, CP ;
Xiong, W ;
Ferrell, JE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (02) :1459-1465
[3]   Positive feedback in eukaryotic gene networks:: cell differentiation by graded to binary response conversion [J].
Becskei, A ;
Séraphin, B ;
Serrano, L .
EMBO JOURNAL, 2001, 20 (10) :2528-2535
[4]   Emergent properties of networks of biological signaling pathways [J].
Bhalla, US ;
Iyengar, R .
SCIENCE, 1999, 283 (5400) :381-387
[5]   Why do protein kinase cascades have more than one level? [J].
Brown, GC ;
Hoek, JB ;
Kholodenko, BN .
TRENDS IN BIOCHEMICAL SCIENCES, 1997, 22 (08) :288-288
[6]   INTERCONVERTIBLE ENZYME CASCADES IN CELLULAR-REGULATION [J].
CHOCK, PB ;
RHEE, SG ;
STADTMAN, ER .
ANNUAL REVIEW OF BIOCHEMISTRY, 1980, 49 :813-843
[7]   Signal transduction by the JNK group of MAP kinases [J].
Davis, RJ .
CELL, 2000, 103 (02) :239-252
[8]  
Davis RJ, 1999, BIOCHEM SOC SYMP, P1
[9]   How responses get more switch like as you move dawn a protein kinase cascade [J].
Ferrell, JE .
TRENDS IN BIOCHEMICAL SCIENCES, 1997, 22 (08) :288-289
[10]   Bistability in cell signaling: How to make continuous processes discontinuous, and reversible processes irreversible [J].
Ferrell, JE ;
Xiong, W .
CHAOS, 2001, 11 (01) :227-236