scholarly journals Integration of Metabolic and Gene Regulatory Networks Modulates the C. elegans Dietary Response

Cell ◽  
2013 ◽  
Vol 153 (6) ◽  
pp. 1406-1407
Author(s):  
Emma Watson ◽  
Lesley T. MacNeil ◽  
H. Efsun Arda ◽  
Lihua Julie Zhu ◽  
Albertha J.M. Walhout
eLife ◽  
2019 ◽  
Vol 8 ◽  
Author(s):  
Yamila N Torres Cleuren ◽  
Chee Kiang Ewe ◽  
Kyle C Chipman ◽  
Emily R Mears ◽  
Cricket G Wood ◽  
...  

Innovations in metazoan development arise from evolutionary modification of gene regulatory networks (GRNs). We report widespread cryptic variation in the requirement for two key regulatory inputs, SKN-1/Nrf2 and MOM-2/Wnt, into the C. elegans endoderm GRN. While some natural isolates show a nearly absolute requirement for these two regulators, in others, most embryos differentiate endoderm in their absence. GWAS and analysis of recombinant inbred lines reveal multiple genetic regions underlying this broad phenotypic variation. We observe a reciprocal trend, in which genomic variants, or knockdown of endoderm regulatory genes, that result in a high SKN-1 requirement often show low MOM-2/Wnt requirement and vice-versa, suggesting that cryptic variation in the endoderm GRN may be tuned by opposing requirements for these two key regulatory inputs. These findings reveal that while the downstream components in the endoderm GRN are common across metazoan phylogeny, initiating regulatory inputs are remarkably plastic even within a single species.


Cell ◽  
2013 ◽  
Vol 153 (1) ◽  
pp. 253-266 ◽  
Author(s):  
Emma Watson ◽  
Lesley T. MacNeil ◽  
H. Efsun Arda ◽  
Lihua Julie Zhu ◽  
Albertha J.M. Walhout

2019 ◽  
Author(s):  
Yamila N. Torres Cleuren ◽  
Chee Kiang Ewe ◽  
Kyle C. Chipman ◽  
Emily Mears ◽  
Cricket G. Wood ◽  
...  

ABSTRACTInnovations in metazoan development arise from evolutionary modification of gene regulatory networks (GRNs). We report widespread cryptic variation in the requirement for two key regulatory inputs, SKN-1/Nrf2 and MOM-2/Wnt, into the C. elegans endoderm GRN. While some natural variants show a nearly absolute requirement for these two regulators, in others, most embryos differentiate endoderm in their absence. GWAS and analysis of recombinant inbred lines reveal multiple genetic regions underlying this broad phenotypic variation. We observe a reciprocal trend, in which genomic variants, or knockdown of endoderm regulatory genes, that result in a high SKN-1 requirement often show low MOM-2/Wnt requirement and vice-versa, suggesting that cryptic variation in the endoderm GRN may be tuned by opposing requirements for these two key regulatory inputs. These findings reveal that while the downstream components in the endoderm GRN are common across metazoan phylogeny, initiating regulatory inputs are remarkably plastic even within a single species.


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