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microPublication / Biology / A quantitative trait locus for...
A quantitative trait locus for nictation behavior on chromosome V
Jun Kim1, Daehan Lee1,2 and Junho Lee1
1Department of Biological Sciences, Institute of Molecular Biology and Genetics, Seoul National University, Seoul 08826, Korea
2Department of Molecular Biosciences, Northwestern University, Evanston, IL, 60208, USA
Correspondence to: Junho Lee (elegans@snu.ac.kr)
Nictation ratio of N2 x CB4856 introgression lines on chromosome V. Note that the genotypes of some of these introgression lines including ysIR50 and ysIR51 are estimates from polymorphism markers, not from whole-genome sequencing. Statistics were analyzed by GraphPad Prism and its One-way ANOVA and Dunnett post-test. All tested groups passed the D'Agostino and Pearson omnibus normality test. Each bar indicates the median of each group. *** P<0.001, significantly different from the control strain, N2.

Description

Lee et al., 2017 showed that CB4856 has a lower nictation ratio (the number of nictating dauers over the number of moving dauers on a micro-dirt chip) than N2, and that a genetic locus (nict-1) on chromosome IV mediates this phenotype difference. Although this paper had no evidence of any other genetic loci for nictation behavior, we have studied other quantitative trait loci (QTL) using different linkage-based mapping strategies. Here, we report another genetic locus that was identified using introgression lines on chromosome V.

N2 x CB4856 introgression lines were tested using a population nictation assay (Lee et al., 2015). We measured the nictation ratios of the ewIR65, ewIR67, ewIR68, and ewIR70 lines, which contain N2-type genome in all chromosomes except for CB4856-type chromosome V segments (Figure 1A). Among them, only ewIR70 line showed significant lower nictation ratio. Therefore, we narrowed down the chromosome V right region.

We also measured nictation ratios of ysIR50, ewIR74, and ysIR51 lines (Figure 1B). ysIR50 and ysIR51 were derived from N2 x ewIR70. ysIR50, ewIR74, and ysIR51 lines showed significantly lower nictation ratios than that of N2. Because the putatively responsible QTL region is covered by another near-isogenic region, eanIR158, which was made independently by Erik Andersen’s laboratory, we measured the nictation ratios of eanIR158 and jyIR3 lines and found that they did not show any significant difference from N2 (Figure 1C).

eanIR158 and jyIR3 lines were built with QX1430 x N2 (personal communication) and QX217 x N2 (Balla et al., 2015), respectively, and QX1430 and QX217 were made by Leonid Kruglyak’s laboratory (Andersen et al., 2015; Rockmen and Kruglyak, 2009). However, ewIR70 and ewIR74 were built by Jan Kammenga’s laboratory (Doroszuk et al., 2009). Thus, we concluded that the two laboratories may have used different N2 or CB4856strain derivatives, which may have altered genetic variations in the introgression lines. A take-home lesson is that it is important to examine NILs derived from common original strains in order to follow QTL without being affected by differences in background genotypes.

Jan Kammenga kindly provided their N2 x CB4856 introgression lines for chromosome V, which include ewIR65, ewIR67, ewIR68, ewIR70, and ewIR74, and Erik Andersen also gave us many introgression lines, which include eanIR158 and jyIR3 covering 15-19 Mb of chromosome V. We appreciate their help.

Reagents

Strains: N2, LJ1250 ysIR50 (V, CB4856>N2), LJ1251 ysIR51 (V, CB4856>N2), ECA238 eanIR158 (V, CB4856, N2), and ERT248 jyIR3 (V, CB4856>N2).

Genotypes: ewIR65 (V, CB4856>N2), ewIR67 (V, CB4856>N2), ewIR68 (V, CB4856>N2), ewIR70 (V, CB4856>N2), and ewIR74 (V, CB4856>N2).

References

Andersen EC, Shimko TC, Crissman JR, Ghosh R, Bloom JS, Seidel HS, et al. A Powerful New Quantitative Genetics Platform, Combining Caenorhabditis elegans High-Throughput Fitness Assays with a Large Collection of Recombinant Strains. G3 (Bethsda). 2015 Mar 13;5(5):911-20.
10.1534/g3.115.017178 | PubMed | PubMed Central
Balla KM, Andersen EC, Kruglyak L, Troemel ER. A Wild C. Elegans Strain Has Enhanced Epithelial Immunity to a Natural Microsporidian Parasite. PLOS Pathog. 2015 Feb 13;11(2):e1004583.
10.1371/journal.ppat.1004583 | PubMed | PubMed Central
Doroszuk A, Snoek LB, Fradin E, Riksen J, Kammenga J. A genome-wide library of CB4856/N2 introgression lines of Caenorhabditis elegans. Nucleic Acids Res. 2009 Sep;37(16):e110.
10.1093/nar/gkp528 | PubMed | PubMed Central
Lee D, Lee H, Choi M-k, Park S, Lee J. Nictation Assays for Caenorhabditis and Other Nematodes. Bio Protoc. 2015 May 4;5(7):e1433.
10.1038/nn.2975 | PubMed
Lee D, Yang H, Kim J, Brady S, Zdraljevic S, Zamanian M, et al. The genetic basis of natural variation in a phoretic behavior. Nat Commun. 2017;8(1):273 PubMed PMID: 28819099.
10.1038/s41467-017-00386-x | PubMed | PubMed Central
Rockman MV, Kruglyak L. Recombinational Landscape and Population Genomics of Caenorhabditis elegans. PLoS Genet. 2009 Mar;5(3):e1000419
PMC2652117 | PubMed | PubMed Central

Funding

This work was supported by the National Research Foundation of Korea (NRF) grants funded by the Korean government (MSIT) (No. 2016K1A3A1A47921615). Jun Kim was supported by POSCO Science Fellowship from the POSCO TJ Park Foundation.

Reviewed By

Erik Andersen

History

Received: August 24, 2017
Accepted: September 13, 2017
Published: September 19, 2017

Copyright

© 2017 by the authors. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Kim, J; Lee, D; Lee, J (2017). A quantitative trait locus for nictation behavior on chromosome V. microPublication Biology. 10.17912/W23D39.
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