Quantitative trait loci and differential gene expression analyses reveal the genetic basis for negatively associated β-carotene and starch content in hexaploid sweetpotato [Ipomoea batatas (L.) Lam.]

0301 basic medicine Amylopectin Plant Roots Gene Biochemistry 630 Agricultural and Biological Sciences Food science Sociology Gene Expression Regulation, Plant sweet potatoes genetics Ipomoea batatas Starch synthase 2. Zero hunger starch carotenoids Life Sciences Starch Chromoplast Orange (colour) General Medicine beta Carotene FOS: Sociology Phenotype 1305 Biotechnology Original Article Biotechnology biotechnology Quantitative trait locus 570 Phytoene synthase Plastid Quantitative Trait Loci Population Environment Horticulture Biosynthesis ipomoea batatas Chloroplast Polyploidy 03 medical and health sciences Quantitative Trait, Heritable 1311 Genetics Genetics 1102 Agronomy and Crop Science Biology Alleles Genetic Association Studies Demography Soil Fertility Botany Cacao Agroforestry Management and Conservation FOS: Biological sciences gene expression Locus (genetics) Amylose Agronomy and Crop Science
DOI: 10.1007/s00122-019-03437-7 Publication Date: 2019-10-08T15:12:23Z
ABSTRACT
AbstractKey messageβ-Carotene content in sweetpotato is associated with theOrangeandphytoene synthasegenes; due to physical linkage ofphytoene synthasewithsucrose synthase, β-carotene and starch content are negatively correlated.AbstractIn populations depending on sweetpotato for food security, starch is an important source of calories, while β-carotene is an important source of provitamin A. The negative association between the two traits contributes to the low nutritional quality of sweetpotato consumed, especially in sub-Saharan Africa. Using a biparental mapping population of 315 F1progeny generated from a cross between an orange-fleshed and a non-orange-fleshed sweetpotato variety, we identified two major quantitative trait loci (QTL) on linkage group (LG) three (LG3) and twelve (LG12) affecting starch, β-carotene, and their correlated traits, dry matter and flesh color. Analysis of parental haplotypes indicated that these two regions acted pleiotropically to reduce starch content and increase β-carotene in genotypes carrying the orange-fleshed parental haplotype at the LG3 locus.Phytoene synthaseandsucrose synthase,the rate-limiting and linked genes located within the QTL on LG3 involved in the carotenoid and starch biosynthesis, respectively, were differentially expressed in Beauregard versus Tanzania storage roots. TheOrangegene, the molecular switch for chromoplast biogenesis, located within the QTL on LG12 while not differentially expressed was expressed in developing roots of the parental genotypes. We conclude that these two QTL regions act together in acisandtransmanner to inhibit starch biosynthesis in amyloplasts and enhance chromoplast biogenesis, carotenoid biosynthesis, and accumulation in orange-fleshed sweetpotato. Understanding the genetic basis of this negative association between starch and β-carotene will inform future sweetpotato breeding strategies targeting sweetpotato for food and nutritional security.
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