Background Crop biofortification is a successful strategy to ameliorate
Vitamin A deficiency. Sorghum is a good candidate for vitamin A
biofortification, as it is a staple food in regions with high prevalence
of vitamin A deficiency. β-carotene—the main provitamin A carotenoid—is
below the target concentration in sorghum grain, therefore,
biofortification breeding is required. Previous studies found evidence
that sorghum carotenoid variation is oligogenic, suggesting that
marker-assisted selection can be an appropriate biofortification method.
However, we hypothesize that sorghum carotenoids have both oligogenic and
polygenic components of variation. Genomics-assisted breeding could
accelerate breeding efforts, but there exists knowledge gaps in the
genetics underlying carotenoid variation, as well as appropriate germplasm
to serve as donors. Results In this study, we characterized carotenoids in
447 accessions from the sorghum association panel and carotenoid panel
using high-performance liquid chromatography, finding high carotenoid
accessions not previously identified. Genome-wide association studies
confirmed that zeaxanthin epoxidase is a major gene underlying variation
for not only zeaxanthin but also lutein and β-carotene. High carotenoid
lines were found to have limited genetic diversity and originated
predominantly from only one country. Potential novel genetic diversity for
carotenoid content was identified through genomic predictions in 2,495
accessions of unexplored germplasm. Oligogenic variation of carotenoids
was confirmed, as well as evidence for polygenic variation, suggesting
both marker-assisted selection and genomic selection can facilitate
breeding efforts. Conclusions Sorghum vitamin A biofortification could be
beneficial for millions of people who rely on it as a dietary staple.
Carotenoid content in sorghum is low, but high heritability suggests that
increasing concentrations through breeding is possible. Low genetic
diversity among high carotenoid lines might be the main limitation for
breeding efforts, therefore further germplasm characterization is needed
to assess the feasibility of biofortification breeding. Based on germplasm
here evaluated, most countries’ germplasm lacks high carotenoid alleles,
thus prebreeding will be needed. An SNP marker within the zeaxanthin
epoxidase gene was identified as a good candidate for use in
marker-assisted selection. Due to the oligogenic and polygenic variation
of sorghum grain carotenoids, both marker-assisted selection and genomic
selection can be employed to accelerate breeding efforts. 1- Ethiopia_NGPS_renamed.vcf
Accessions and SNP dataset from the NPGS
Ethiopian collection were obtained from Cuevas, H. E. via personal
communication. The dataset consists of 367 accessions and 215,741 SNPs on
version 3.1 of the sorghum genome. Original data is from: Cuevas, H.E., Rosa-Valentin,
G., Hayes, C.M., Rooney, W.L. and Hoffman, L. Genomic characterization of
a core set of the USDA-NPGS Ethiopian sorghum germplasm collection:
implications for germplasm conservation, evaluation, and utilization in
crop improvement. BMC Genomics 18:108. 2017.
2- Sudan_NGPS_renamed.vcf Accessions and SNP dataset from the NPGS Sudan core
collection were obtained from Cuevas, H. E. via personal communication.
The dataset consists of 319 accessions and 215,741 SNPs on version 3.1 of
the sorghum genome. Original data
is from: Cuevas, H.E. and Prom, L.K. Evaluation of genetic diversity,
agronomic traits, and anthracnose resistance in the NPGS Sudan sorghum
core collection. BMC Genomics 21:88. 2020.