» Articles » PMID: 28163598

SSR Marker-assisted Screening of Commercial Tomato Genotypes Under Salt Stress

Overview
Journal Breed Sci
Date 2017 Feb 7
PMID 28163598
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Salt stress was applied to tomato commercial genotypes to study adverse effects on their phenotypic traits. Three were saline tolerant (San Miguel, Romelia and Llanero), two were mildly tolerant (Perfect peel HF1 and Heinz 1350) whereas the remaining were sensitive. Genotyping cultivars using 19 polymorphic SSRs out of 25 tested produced a total of 70 alleles with an average of 3.68 alleles per locus and PIC values ranging from 0.22 (SSR 26, 92, 66 and TG35) to 0.82 (SSR 356). Principal component analysis (PCA) showed two contrasting panels discriminating tolerant and sensitive groups and one panel with scattered genotypes. STRUCTURE analysis clustered genotypes within three groups in accordance with their salt stress behavior. The success of tomato salt-tolerance breeding programs can be enhanced through molecular characterization of diversity within commercial cultivars that adapt differently to stress conditions. To this end, we combined phenotypes and SSR marker-genotypes to seek sources of salt tolerance that might be tomato species-specific. We integrated and represented genotype-phenotype associations from multiple loci into a multi-layer network representation. It is a systemic view linking discriminating genotypes to salt stress phenotypes, which may guide strategies for the introgression of valuable traits in target tomato varieties to overcome salinity.

Citing Articles

Characterization of Lithuanian Tomato Varieties and Hybrids Using Phenotypic Traits and Molecular Markers.

Radzevicius A, Siksnianiene J, Karkleliene R, Juskeviciene D, Antanyniene R, Misiukevicius E Plants (Basel). 2024; 13(15).

PMID: 39124261 PMC: 11314498. DOI: 10.3390/plants13152143.


Plant-on-a-chip: continuous, soilless electrochemical monitoring of salt uptake and tolerance among different genotypes of tomato.

Coatsworth P, Cotur Y, Asfour T, Zhou Z, Flauzino J, Bozkurt T Sens Diagn. 2024; 3(5):799-808.

PMID: 38766392 PMC: 11097007. DOI: 10.1039/d4sd00065j.


Tomato salt tolerance mechanisms and their potential applications for fighting salinity: A review.

Guo M, Wang X, Guo H, Bai S, Khan A, Wang X Front Plant Sci. 2022; 13:949541.

PMID: 36186008 PMC: 9515470. DOI: 10.3389/fpls.2022.949541.


Advances in Understanding and Harnessing the Molecular Regulatory Mechanisms of Vegetable Quality.

Gao L, Hao N, Wu T, Cao J Front Plant Sci. 2022; 13:836515.

PMID: 35371173 PMC: 8964363. DOI: 10.3389/fpls.2022.836515.


Genome-Wide Survey and Development of the First Microsatellite Markers Database () in L.

Martina M, Acquadro A, Barchi L, Gulino D, Brusco F, Rabaglio M Int J Mol Sci. 2022; 23(6).

PMID: 35328546 PMC: 8949970. DOI: 10.3390/ijms23063126.


References
1.
Botstein D, White R, Skolnick M, Davis R . Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am J Hum Genet. 1980; 32(3):314-31. PMC: 1686077. View

2.
Hasanuzzaman M, Nahar K, Alam M, Bhowmik P, Hossain M, Rahman M . Potential use of halophytes to remediate saline soils. Biomed Res Int. 2014; 2014:589341. PMC: 4109415. DOI: 10.1155/2014/589341. View

3.
Cao X, Wu Z, Zhou R, Jiang F, Yang Z . A novel random amplified polymorphic DNA-based strategy for genetic diversity analysis and identification of tomatoes. Genet Mol Res. 2015; 14(1):1650-61. DOI: 10.4238/2015.March.6.11. View

4.
Cline M, Smoot M, Cerami E, Kuchinsky A, Landys N, Workman C . Integration of biological networks and gene expression data using Cytoscape. Nat Protoc. 2007; 2(10):2366-82. PMC: 3685583. DOI: 10.1038/nprot.2007.324. View

5.
Zhou H, Hanson T, Zhang J . Generalized accelerated failure time spatial frailty model for arbitrarily censored data. Lifetime Data Anal. 2016; 23(3):495-515. PMC: 5352560. DOI: 10.1007/s10985-016-9361-4. View