Data from: Solanum pennellii (LA5240) backcross inbred lines (BILs) for high resolution mapping in tomato
Data files
Jan 17, 2024 version files 29.70 MB
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Genotype_Phenotype.LEA.csv
22.06 MB
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Genotype_Phenotype.TOP.csv
7.64 MB
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README.md
1.84 KB
Abstract
Wild species are an invaluable source of new traits for crop improvement. Over the years the tomato community bred cultivated lines that carry introgressions from different species of the tomato tribe to facilitate trait discovery and mapping. The next phase in such projects is to find the genes that drive the identified phenotypes. This can be achieved by genotyping a few thousand individuals resulting in fine-mapping that can potentially identify the causative gene. To couple trait discovery and fine mapping we are presenting large, recombination-rich, Backcross Inbred Line (BIL) populations involving an unexplored accession of the wild, green-fruited species Solanum pennellii (LA5240; the Lost Accession) with two modern tomato inbreds: LEA, determinate, and TOP indeterminate. The LEA and TOP BILs are in BC2F6-8 generation and include 1,400 and 500 lines respectively. The BILs were genotyped with ~5,000 SPET markers, showing that in the euchromatic regions there was one recombinant every 17-18 Kb while in the heterochromatin a recombinant every 600-700 Kb (TOP and LEA respectively). To gain perspective on the topography of recombination we compared five independent members of the self-pruning gene family with their respective neighboring genes; based on PCR markers, in all cases we found recombinants. Further mapping analysis of two known morphological mutations that segregated in the BILs (Self-pruning and Hair), showed that the maximal delimited intervals were 73 Kb and 210 Kb respectively and included the known causative genes. The LOST_BILs provide a solid framework to study traits derived from a tolerant wild tomato.
Author(s):
Shai Torgeman
The Hebrew University of Jerusalem
Faculty of Agriculture
Institute of Plant Sciences
P.O.Box 12, Rehovot 76100, Israel
shai.torgeman@mail.huji.ac.il
Dani Zamir
The Hebrew University of Jerusalem
Faculty of Agriculture
Institute of Plant Sciences
P.O.Box 12, Rehovot 76100, Israel
dani.zamir@mail.huji.ac.il
File list:
Genotype&Phenotype.LEA.csv
Genotype&Phenotype.TOP.csv
Rqtl.txt
Files descriptions:
Genotype&Phenotype.LEA/TOP - Genotypic data for all the BILs population got from Single Primer Enrichment Technology (SPET).
The first row refer to the marker name and its physical position.
The second row refer to the chromosome number.
the third row refer to the genetic distance(CM) calculated from the number of recombination between neighbor markers.
NA are missing genotype data points
genotype = 1 refer to cultivated allele
genotype = 3 refer to wild species allele
Throughout the autumn 2017, the LEA BILs (1389) and the TOP BILs (490) were grown in a greenhouse in Chatzav, Israel and scored for plant habit (determinate and indeterminate) and hairiness on stem (Hairy and hair absent).
Genome scan for trait mapping analysis in the bi-parental populations was performed in R/qtl and R/qtl2 packages (Broman et al., 2003) by Haley-Knott regression (Haley & Knott, 1992) and validated using single marker analysis (ANOVA) in JMP pro 16 software (SAS Institute, Cary, NC, USA).
The Genotype and Phenotypes data combined for upload in R format for QTL analysis. script add in R file.
Rqtl.R - script for QTL analysis Genotype&Phenotype.csv file.
notes:
Our analysis done by combine of R software to detect the QTLs and by JMP software for the t-test and multiple comparisons analysis.