Abstract:A melon (Cucumis melo L.) genomic library of near-isogenic lines derived from the cross between the Spanish cultivar Piel de Sapo and the exotic accession PI 161375 has been evaluated for fruit quality traits in four different locations. Traits evaluated were fruit weight, soluble solids content, maximum fruit diameter, fruit length, fruit shape index, ovary shape index, external color, and flesh color. Among these traits, soluble solids content showed the highest genotype × … Show more
“…Recently, Feder et al [71] identified a Kelch domain-containing F-box protein regulating naringenin chalcone accumulation in melon rind producing the change from white to yellow rind. This gene (MELO3C011980, annotated as similar to F-box/kelch-repeat protein At1g23390) colocalizes with QTLs involved in the variation of external color in melons [72, 73]. In C. pepo , we found two genes annotated as F-box/kelch-repeat protein (Additional file 6) in the LOD peak regions of the MaRCo_4 QTL (CP32_ scaffold000022_600093-603383 and 624476-611084, best nr hit F-box/kelch-repeat protein At1g55270-like and At2g44130-like respectively).…”
Section: Resultsmentioning
confidence: 99%
“…Other two minor QTLs (R 2 < 5%) involved in the variation of flesh color were also detected, although with significant E and G x E effect (Additional file 5) ( MaFCo_10 , 37.9 cM, CP32_scaffold000009_1923620-CP32_scaffold000009_2317405, and MaFCo_13 , 53.1 cM, CP32_scaffold000017_2743863-CP32_scaffold000108_169208) that can act modulating the effect of the major gene, as it has been also reported in melons [72, 73, 78–80]. …”
Background
Cucurbita pepo is a cucurbit with growing economic importance worldwide. Zucchini morphotype is the most important within this highly variable species. Recently, transcriptome and Simple Sequence Repeat (SSR)- and Single Nucleotide Polymorphism (SNP)-based medium density maps have been reported, however further genomic tools are needed for efficient molecular breeding in the species. Our objective is to combine currently available complete transcriptomes and the Zucchini genome sequence with high throughput genotyping methods, mapping population development and extensive phenotyping to facilitate the advance of genomic research in this species.ResultsWe report the Genotyping-by-sequencing analysis of a RIL population developed from the inter subspecific cross Zucchini x Scallop (ssp. pepo x ssp. ovifera). Several thousands of SNP markers were identified and genotyped, followed by the construction of a high-density linkage map based on 7,718 SNPs (average of 386 markers/linkage group) covering 2,817.6 cM of the whole genome, which is a great improvement with respect to previous maps. A QTL analysis was performed using phenotypic data obtained from the RIL population from three environments. In total, 48 consistent QTLs for vine, flowering and fruit quality traits were detected on the basis of a multiple-environment analysis, distributed in 33 independent positions in 15 LGs, and each QTL explained 1.5–62.9% of the phenotypic variance. Eight major QTLs, which could explain greater than 20% of the phenotypic variation were detected and the underlying candidate genes identified.ConclusionsHere we report the first SNP saturated map in the species, anchored to the physical map. Additionally, several consistent QTLs related to early flowering, fruit shape and length, and rind and flesh color are reported as well as candidate genes for them. This information will enhance molecular breeding in C. pepo and will assist the gene cloning underlying the studied QTLs, helping to reveal the genetic basis of the studied processes in squash.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-016-3439-y) contains supplementary material, which is available to authorized users.
“…Recently, Feder et al [71] identified a Kelch domain-containing F-box protein regulating naringenin chalcone accumulation in melon rind producing the change from white to yellow rind. This gene (MELO3C011980, annotated as similar to F-box/kelch-repeat protein At1g23390) colocalizes with QTLs involved in the variation of external color in melons [72, 73]. In C. pepo , we found two genes annotated as F-box/kelch-repeat protein (Additional file 6) in the LOD peak regions of the MaRCo_4 QTL (CP32_ scaffold000022_600093-603383 and 624476-611084, best nr hit F-box/kelch-repeat protein At1g55270-like and At2g44130-like respectively).…”
Section: Resultsmentioning
confidence: 99%
“…Other two minor QTLs (R 2 < 5%) involved in the variation of flesh color were also detected, although with significant E and G x E effect (Additional file 5) ( MaFCo_10 , 37.9 cM, CP32_scaffold000009_1923620-CP32_scaffold000009_2317405, and MaFCo_13 , 53.1 cM, CP32_scaffold000017_2743863-CP32_scaffold000108_169208) that can act modulating the effect of the major gene, as it has been also reported in melons [72, 73, 78–80]. …”
Background
Cucurbita pepo is a cucurbit with growing economic importance worldwide. Zucchini morphotype is the most important within this highly variable species. Recently, transcriptome and Simple Sequence Repeat (SSR)- and Single Nucleotide Polymorphism (SNP)-based medium density maps have been reported, however further genomic tools are needed for efficient molecular breeding in the species. Our objective is to combine currently available complete transcriptomes and the Zucchini genome sequence with high throughput genotyping methods, mapping population development and extensive phenotyping to facilitate the advance of genomic research in this species.ResultsWe report the Genotyping-by-sequencing analysis of a RIL population developed from the inter subspecific cross Zucchini x Scallop (ssp. pepo x ssp. ovifera). Several thousands of SNP markers were identified and genotyped, followed by the construction of a high-density linkage map based on 7,718 SNPs (average of 386 markers/linkage group) covering 2,817.6 cM of the whole genome, which is a great improvement with respect to previous maps. A QTL analysis was performed using phenotypic data obtained from the RIL population from three environments. In total, 48 consistent QTLs for vine, flowering and fruit quality traits were detected on the basis of a multiple-environment analysis, distributed in 33 independent positions in 15 LGs, and each QTL explained 1.5–62.9% of the phenotypic variance. Eight major QTLs, which could explain greater than 20% of the phenotypic variation were detected and the underlying candidate genes identified.ConclusionsHere we report the first SNP saturated map in the species, anchored to the physical map. Additionally, several consistent QTLs related to early flowering, fruit shape and length, and rind and flesh color are reported as well as candidate genes for them. This information will enhance molecular breeding in C. pepo and will assist the gene cloning underlying the studied QTLs, helping to reveal the genetic basis of the studied processes in squash.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-016-3439-y) contains supplementary material, which is available to authorized users.
“…(Group Inodorus)] genome (Eduardo, Arús, & Monforte, 2005) used in this study was described by Eduardo et al (2007). Eighteen NILs contained a single molecular markerdefined introgression from SC into the PS genetic background (Eduardo et al, 2007), and the rest had two or more. The introgressions from SC presented in this set of NILs covered at least 85% of melon genome.…”
Section: Plant Materialsmentioning
confidence: 99%
“…NILs were coded with the prefix ''SC" followed by x-y numbers and, in some cases, one or two z letters (SCx-y z, for example SC3-5ab): the first x number indicates the linkage group (LG), and the second number y indicates the number of the NIL within the LG. The letters indicates additional genetic facts: ''a", there is more than one introgression; ''b" the NIL has an introgression slightly different from the introgression of the NIL with the same number described in Eduardo et al (2005), although it covers the same genomic region; ''h", the introgression is heterozygous and ''d", part of the introgression is heterozygous (Eduardo et al, 2007). Although the mapping resolution of this population is not very high, it is sufficient for focusing research effort.…”
a b s t r a c tThis paper characterizes the aroma volatile profile found in a collection of near-isogenic lines (NILs) of melon (Cucumis melo L.) obtained by solid-phase microextraction and analyzed by gas chromatography-mass spectrometry. The collection was built with introgressions of an exotic accession (PI 161375) into the parental line 'Piel de sapo' (PS) and was useful for mapping quantitative trait loci (QTLs) associated with melon flesh aroma. The aroma profile was composed of 24 compounds detected in PS or the NILs: three esters, six aldehydes, three alkanes, three aromatic hydrocarbons, two terpenes, two ketones, one alcohol, one sulphur-derived compound, one cyclic branched alkene, one naphthalene and one ether. Hexanal showed the highest relative concentration in the collection, followed by camphor and methanethiolate with no difference between PS and the NILs. These results allowed us to map four QTLs in linkage groups IV, VIII and XI associated with the formation of 3-hydroxy-2,4,4-trimethylpentyl 2-methylpropanoate, octanal and (Z,Z)-3,6-nonadienal.
“…SSR markers fromDanin-Poleg et al (2000, 2001), Fazio et al (2002,Chiba et al (2003),Ritchel et al (2004),Gonzalo et al (2005),Kong et al (2006Kong et al ( , 2007 andFukino et al (2007) b Linkage group number according toPerin et al (2002),Eduardo et al (2007),Cuevas et al (2008) andFukino et al …”
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