TY - JOUR
T1 - Production of abnormal proteins in E. coli stimulates transcription of ion and other heat shock genes
AU - Goff, Stephen A.
AU - Goldberg, Alfred L.
N1 - Funding Information:
The authors are very grateful to M Rosa for her expert advice and her assistance, especially in the experiments with TPA. We are also grateful to M. Rosa and B. Wallner-Philip for providing piasmids encoding for TPA, TPA fragments, and HSA. We thank Dr. Richard Flavelt for his interest and encouragement, and Mrs. Lynette M, Oliphant and Mrs. Aurora Scott for their very valuable assistance in preparing this manuscript. These studies were supported by grants from Biogen, Inc. and the National Institute of Neurological Disease and Stroke. During the course of this work, S. G. was supported by a Biogen Fellowship and an Albert Ryan Fellowship.
PY - 1985/6
Y1 - 1985/6
N2 - The product of the Ion gene in Escherichia coli, protease La, plays an important role in the degradation of abnormal proteins. To determine whether the presence of abnormal proteins stimulates expression of this gene, we examined its transcription using a Ion-IacZ operon fusion. After the cells synthesized large amounts of aberrant polypeptides (e.g. following incorporation of the arginine analog, canavanine, or production of incomplete proteins with puromycin, or induction of translational errors with streptomycin), these cells showed a two to three fold increase in Ion-IacZ expression. Furthermore, synthesis of a single cloned protein, e.g. human tissue plasminogin activator, caused a similar increase in Ion transcription. This induction of Ion by abnormal proteins requires the heat shock regulatory gene htpR and was not seen in htpR- cells. Under these various conditions, other heat shock proteins were also induced. Thus, the appearance of aberrant cell proteins may be a common signal under many adverse conditions for the induction of cell protease (or proteases) and other heat shock proteins.
AB - The product of the Ion gene in Escherichia coli, protease La, plays an important role in the degradation of abnormal proteins. To determine whether the presence of abnormal proteins stimulates expression of this gene, we examined its transcription using a Ion-IacZ operon fusion. After the cells synthesized large amounts of aberrant polypeptides (e.g. following incorporation of the arginine analog, canavanine, or production of incomplete proteins with puromycin, or induction of translational errors with streptomycin), these cells showed a two to three fold increase in Ion-IacZ expression. Furthermore, synthesis of a single cloned protein, e.g. human tissue plasminogin activator, caused a similar increase in Ion transcription. This induction of Ion by abnormal proteins requires the heat shock regulatory gene htpR and was not seen in htpR- cells. Under these various conditions, other heat shock proteins were also induced. Thus, the appearance of aberrant cell proteins may be a common signal under many adverse conditions for the induction of cell protease (or proteases) and other heat shock proteins.
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U2 - 10.1016/S0092-8674(85)80031-3
DO - 10.1016/S0092-8674(85)80031-3
M3 - Article
C2 - 3886165
AN - SCOPUS:0022344755
SN - 0092-8674
VL - 41
SP - 587
EP - 595
JO - Cell
JF - Cell
IS - 2
ER -