Faculty Opinions recommendation of Natural variation in the npr-1 gene modifies ethanol responses of wild strains of C. elegans.

Author(s):  
Jonathan Hodgkin
Neuron ◽  
2004 ◽  
Vol 42 (5) ◽  
pp. 731-743 ◽  
Author(s):  
Andrew G Davies ◽  
Jill C Bettinger ◽  
Tod R Thiele ◽  
Meredith E Judy ◽  
Steven L McIntire

2019 ◽  
Author(s):  
Amy K. Webster ◽  
Anthony Hung ◽  
Brad T. Moore ◽  
Ryan Guzman ◽  
James M. Jordan ◽  
...  

ABSTRACTTo understand the genetic basis of complex traits, it is important to be able to efficiently phenotype many genetically distinct individuals. In the nematode Caenorhabditis elegans, individuals have been isolated from diverse populations around the globe and whole-genome sequenced. As a result, hundreds of wild strains with known genome sequences can be used for genome-wide association studies (GWAS). However, phenotypic analysis of these strains can be laborious, particularly for quantitative traits requiring multiple measurements per strain. Starvation resistance is likely a fitness-proximal trait for nematodes, and it is related to metabolic disease risk in humans. However, natural variation in C. elegans starvation resistance has not been characterized, and precise measurement of the trait is time-intensive. Here, we developed a population selection and sequencing-based approach to phenotype starvation resistance in a pool of 96 wild strains. We used restriction site-associated DNA sequencing (RAD-seq) to infer the frequency of each strain among survivors in a mixed culture over time during starvation. We used manual starvation survival assays to validate the trait data, confirming that strains that increased in frequency over time are starvation-resistant relative to strains that decreased in frequency. These results document natural variation in starvation resistance. Further, we found that variation in starvation resistance is significantly associated with variation at a region on chromosome III. Using a near-isogenic line (NIL), we showed the importance of this genomic interval for starvation resistance. This study demonstrates the feasibility of using population selection and sequencing in an animal model for phenotypic analyses of quantitative traits, reveals natural variation of starvation resistance in C. elegans, and identifies a genomic region that contributes to such variation.


2019 ◽  
Vol 9 (10) ◽  
pp. 3477-3488 ◽  
Author(s):  
Amy K. Webster ◽  
Anthony Hung ◽  
Brad T. Moore ◽  
Ryan Guzman ◽  
James M. Jordan ◽  
...  

To understand the genetic basis of complex traits, it is important to be able to efficiently phenotype many genetically distinct individuals. In the nematode Caenorhabditis elegans, individuals have been isolated from diverse populations around the globe and whole-genome sequenced. As a result, hundreds of wild strains with known genome sequences can be used for genome-wide association studies (GWAS). However, phenotypic analysis of these strains can be laborious, particularly for quantitative traits requiring multiple measurements per strain. Starvation resistance is likely a fitness-proximal trait for nematodes, and it is related to metabolic disease risk in humans. However, natural variation in C. elegans starvation resistance has not been systematically characterized, and precise measurement of the trait is time-intensive. Here, we developed a population-selection-and-sequencing-based approach to phenotype starvation resistance in a pool of 96 wild strains. We used restriction site-associated DNA sequencing (RAD-seq) to infer the frequency of each strain among survivors in a mixed culture over time during starvation. We used manual starvation survival assays to validate the trait data, confirming that strains that increased in frequency over time are starvation-resistant relative to strains that decreased in frequency. Further, we found that variation in starvation resistance is significantly associated with variation at a region on chromosome III. Using a near-isogenic line (NIL), we showed the importance of this genomic interval for starvation resistance. This study demonstrates the feasibility of using population selection and sequencing in an animal model for phenotypic analysis of quantitative traits, documents natural variation of starvation resistance in C. elegans, and identifies a genomic region that contributes to such variation.


2021 ◽  
Author(s):  
Janneke Wit ◽  
Steffen R. Hahnel ◽  
Briana C. Rodriguez ◽  
Erik Andersen

Treatment of parasitic nematode infections depends primarily on the use of anthelmintics. However, this drug arsenal is limited, and resistance against most anthelmintics is widespread. Emodepside is a new anthelmintic drug effective against gastrointestinal and filarial nematodes. Nematodes that are resistant to other anthelmintic drug classes are susceptible to emodepside, indicating that the emodepside mode of action is distinct from previous anthelmintics. The laboratory-adapted Caenorhabditis elegans strain N2 is sensitive to emodepside, and genetic selection and in vitro experiments implicated slo-1, a BK potassium channel gene, in emodepside mode of action. In an effort to understand how natural populations will respond to emodepside, we measured brood sizes and developmental rates of wild C. elegans strains after exposure to the drug and found natural variation across the species. Some variation in emodepside responses can be explained by natural differences in slo-1. This result suggests that other genes in addition to slo-1 underlie emodepside resistance in wild C. elegans strains. Additionally, all assayed strains have higher offspring production in low concentrations of emodepside (a hormetic effect), which could impact treatment strategies. We find that natural variation affects emodepside sensitivity, supporting the suitability of C. elegans as a model system to study emodepside responses across parasitic nematodes.


PLoS Genetics ◽  
2020 ◽  
Vol 16 (8) ◽  
pp. e1008984
Author(s):  
Huimin Na ◽  
Stefan Zdraljevic ◽  
Robyn E. Tanny ◽  
Albertha J. M. Walhout ◽  
Erik C. Andersen

Science ◽  
2012 ◽  
Vol 335 (6068) ◽  
pp. 574-578 ◽  
Author(s):  
R. Ghosh ◽  
E. C. Andersen ◽  
J. A. Shapiro ◽  
J. P. Gerke ◽  
L. Kruglyak

2015 ◽  
Vol 25 (20) ◽  
pp. 2730-2737 ◽  
Author(s):  
Luke M. Noble ◽  
Audrey S. Chang ◽  
Daniel McNelis ◽  
Max Kramer ◽  
Mimi Yen ◽  
...  

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