TY - JOUR
T1 - Sequencing-based bin map construction of a tomato mapping population, facilitating high-resolution quantitative trait loci detection
AU - Gonda, Itay
AU - Ashrafi, Hamid
AU - Lyon, David A.
AU - Strickler, Susan R.
AU - Hulse-Kemp, Amanda M.
AU - Ma, Qiyue
AU - Sun, Honghe
AU - Stoffel, Kevin
AU - Powell, Adrian F.
AU - Futrell, Stephanie
AU - Thannhauser, Theodore W.
AU - Fei, Zhangjun
AU - Van Deynze, Allen E.
AU - Mueller, Lukas A.
AU - Giovannoni, James J.
AU - Foolad, Majid R.
N1 - Funding Information:
We want to thank Dr. Jennifer Spindel from the lab of Prof. Susan McCouch for invaluable assistance with the R/qtl script. We also graciously thank all former Penn State staff, graduate and undergraduate students, in particular Dr. Matthew Kinkade, who helped with the RIL and NIL populations development, RFLP mapping, and QTL analysis for fruit quality characteristics. This research was supported in part by BARD, the United States–Israel Binational Agricultural Research and Development Fund, Vaadia-BARD Postdoctoral Fellowship Award No. FI-508-14 to IG; National Science Foundation Plant Genome Program grant IOS-1539831 to ZF and JJG; USDA–Agricultural Research Service funded project number 301-8062-21000-037-00D to JJG and TWT; and USDA–National Institute for Food and Agriculture, Award no. 2009-85606-05673 to PIs for the Solanaceae Coordinated Project, David Douches and C. Robin Buell, Michigan State University, Walter De Jong, Cornell University, David Francis, The Ohio State University, and AVD for supporting GBS for this work.
Publisher Copyright:
© Crop Science Society of America.
PY - 2019/3
Y1 - 2019/3
N2 - Genotyping-by-sequencing (GBS) was employed to construct a highly saturated genetic linkage map of a tomato (Solanum lycopersicum L.) recombinant inbred line (RIL) population, derived from a cross between cultivar NC EBR-1 and the wild tomato S. pimpinellifolium L. accession LA2093. A pipeline was developed to convert single nucleotide polymorphism (SNP) data into genomic bins, which could be used for fine mapping of quantitative trait loci (QTL) and identification of candidate genes. The pipeline, implemented in a python script named SNPbinner, adopts a hidden Markov model approach for calculation of recombination breakpoints followed by genomic bins construction. The total length of the newly developed high-resolution genetic map was 1.2-fold larger than previously estimated based on restriction fragment length polymorphism (RFLP) and polymerase chain reaction (PCR)–based markers. The map was used to verify and refine QTL previously identified for two fruit quality traits in the RIL population, fruit weight (FW) and fruit lycopene content (LYC). Two well-described FW QTL (fw2.2 and fw3.2) were localized precisely at their known underlying causative genes, and the QTL intervals were decreased by two- to tenfold. A major QTL for LYC content (Lyc12.1) was verified at high resolution and its underlying causative gene was determined to be z-carotene isomerase (SlZISO). The RIL population, the high resolution genetic map, and the easy-to-use genotyping pipeline, SNPbinner, are made publicly available.
AB - Genotyping-by-sequencing (GBS) was employed to construct a highly saturated genetic linkage map of a tomato (Solanum lycopersicum L.) recombinant inbred line (RIL) population, derived from a cross between cultivar NC EBR-1 and the wild tomato S. pimpinellifolium L. accession LA2093. A pipeline was developed to convert single nucleotide polymorphism (SNP) data into genomic bins, which could be used for fine mapping of quantitative trait loci (QTL) and identification of candidate genes. The pipeline, implemented in a python script named SNPbinner, adopts a hidden Markov model approach for calculation of recombination breakpoints followed by genomic bins construction. The total length of the newly developed high-resolution genetic map was 1.2-fold larger than previously estimated based on restriction fragment length polymorphism (RFLP) and polymerase chain reaction (PCR)–based markers. The map was used to verify and refine QTL previously identified for two fruit quality traits in the RIL population, fruit weight (FW) and fruit lycopene content (LYC). Two well-described FW QTL (fw2.2 and fw3.2) were localized precisely at their known underlying causative genes, and the QTL intervals were decreased by two- to tenfold. A major QTL for LYC content (Lyc12.1) was verified at high resolution and its underlying causative gene was determined to be z-carotene isomerase (SlZISO). The RIL population, the high resolution genetic map, and the easy-to-use genotyping pipeline, SNPbinner, are made publicly available.
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U2 - 10.3835/plantgenome2018.02.0010
DO - 10.3835/plantgenome2018.02.0010
M3 - Article
C2 - 30951101
AN - SCOPUS:85064268030
VL - 12
JO - Plant Genome
JF - Plant Genome
SN - 1940-3372
IS - 1
M1 - 180010
ER -