2013
DOI: 10.2135/cropsci2013.03.0132
|View full text |Cite
|
Sign up to set email alerts
|

Three Quantitative Trait Loci Conferring Resistance to Kernel Fissuring in Rice Identified by Selective Genotyping in Two Tropical Japonica Populations

Abstract: Kernel fissures in rice (Oryza sativa L.) caused by pre‐ or postharvest stresses are the leading cause of breakage among milled rice, causing economic losses for producers, millers, and processors. The present study identified three quantitative trait loci (QTLs) associated with fissure resistance (FisR) through selective genotyping of two mapping populations, one derived from ‘Cypress’ × ‘LaGrue’ and the other derived from ‘Cybonnet’ × ‘Saber’. Two QTLs were identified on chromosome 1 and one on chromosome 8 … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

3
44
0

Year Published

2018
2018
2022
2022

Publication Types

Select...
4
2

Relationship

1
5

Authors

Journals

citations
Cited by 17 publications
(47 citation statements)
references
References 20 publications
3
44
0
Order By: Relevance
“…Five QTLs affecting rates of kernel fissuring were identified (Table 2). The three with the largest LODs and additive effects among the CS‐RILs ( qFIS1‐1 , qFIS1‐2 , and qFIS8) were the same three FR loci discovered previously in Cypress (Pinson et al, 2013). Cypress is the sole FR parent of Cybonnet, and thus it was not surprising for Cybonnet to have seemingly inherited its three FR alleles from Cypress.…”
Section: Resultssupporting
confidence: 80%
See 4 more Smart Citations
“…Five QTLs affecting rates of kernel fissuring were identified (Table 2). The three with the largest LODs and additive effects among the CS‐RILs ( qFIS1‐1 , qFIS1‐2 , and qFIS8) were the same three FR loci discovered previously in Cypress (Pinson et al, 2013). Cypress is the sole FR parent of Cybonnet, and thus it was not surprising for Cybonnet to have seemingly inherited its three FR alleles from Cypress.…”
Section: Resultssupporting
confidence: 80%
“…The next largest marker gap is a 44‐cM gap on chromosome 3, which was also characterized as likely IBD with eight intervening SNP and SSR loci being monomorphic. Although SNP monomorphism supported contentions of IBD in some chromosomal regions, in other regions polymorphic SNPs were now available to support new QTL evaluations in regions previously confounded by SSR monomorphism (Pinson et al, 2013). This was most notable on the short arms of chromosomes 1 and 8, where qFIS1‐1 and qFIS8 were detected with SSRs, but not mapped precisely (Pinson et al, 2013).…”
Section: Resultsmentioning
confidence: 99%
See 3 more Smart Citations