TY - JOUR
T1 - Subtle alterations in PCNA-partner interactions severely impair DNA replication and repair
AU - Fridman, Yearit
AU - Palgi, Niv
AU - Dovrat, Daniel
AU - Ben-Aroya, Shay
AU - Hieter, Philip
AU - Aharoni, Amir
PY - 2010/10
Y1 - 2010/10
N2 - The robustness of complex biological processes in the face of environmental and genetic perturbations is a key biological trait. However, while robustness has been extensively studied, little is known regarding the fragility of biological processes. Here, we have examined the susceptibility of DNA replication and repair processes mediated by the proliferating cell nuclear antigen (PCNA). Using protein directed evolution, biochemical, and genetic approaches, we have generated and characterized PCNA mutants with increased affinity for several key partners of the PCNA-partner network. We found that increases in PCNA-partner interaction affinities led to severe in vivo phenotypic defects. Surprisingly, such defects are much more severe than those induced by complete abolishment of the respective interactions. Thus, the subtle and tunable nature of these affinity perturbations produced different phenotypic effects than realized with traditional "on-off" analysis using gene knockouts. Our findings indicate that biological systems can be robust to one set of perturbations yet fragile to others.
AB - The robustness of complex biological processes in the face of environmental and genetic perturbations is a key biological trait. However, while robustness has been extensively studied, little is known regarding the fragility of biological processes. Here, we have examined the susceptibility of DNA replication and repair processes mediated by the proliferating cell nuclear antigen (PCNA). Using protein directed evolution, biochemical, and genetic approaches, we have generated and characterized PCNA mutants with increased affinity for several key partners of the PCNA-partner network. We found that increases in PCNA-partner interaction affinities led to severe in vivo phenotypic defects. Surprisingly, such defects are much more severe than those induced by complete abolishment of the respective interactions. Thus, the subtle and tunable nature of these affinity perturbations produced different phenotypic effects than realized with traditional "on-off" analysis using gene knockouts. Our findings indicate that biological systems can be robust to one set of perturbations yet fragile to others.
UR - http://www.scopus.com/inward/record.url?scp=78149392991&partnerID=8YFLogxK
U2 - 10.1371/journal.pbio.1000507
DO - 10.1371/journal.pbio.1000507
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C2 - 20967232
AN - SCOPUS:78149392991
SN - 1544-9173
VL - 8
JO - PLoS Biology
JF - PLoS Biology
IS - 10
M1 - e1000507
ER -