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Hinze, L. L.

Publications and source records attributed to Hinze, L. L..

2 recordsLinked to original sources

Comparative multi-omic analyses reveal gene regulatory networks controlling physiological and metabolic responses to drought in upland cotton

Drought stress substantially impacts crop physiology resulting in alteration of growth and productivity. Understanding the genetic and molecular crosstalk between stress responses and agronomically important traits such as fiber yield is particularly complicated in the allopolyploid species, upland cotton (Gossypium hirsutum), due to reduced sequence variability between A and D subgenomes. To better understand how drought stress impacts yield, the transcriptomes of 22 genetically and phenotypically diverse upland cotton accessions grown under well-watered and water-limited conditions in the Arizona low desert were sequenced. Gene co-expression analyses were performed, uncovering a group of stress response genes, in particular transcription factors GhDREB2A-A and GhHSFA6B-D, associated with improved yield under water-limited conditions in an ABA-independent manner. DNA affinity purification sequencing (DAP-seq), as well as public cistrome data from Arabidopsis, were used to identify targets of these two TFs. Among these targets were two lint-yield associated genes previously identified through genome-wide association studies (GWAS) -based approaches, GhABP-D and GhIPS1-A. Biochemical and phylogenetic approaches were used to determine that GhIPS1-A is positively regulated by GhHSFA6B-D, and that this regulatory mechanism is specific to Gossypium spp. containing the A (old-world) genome. Finally, a SNP was identified within the GhHSFA6B-D binding site in GhIPS1-A that is positively associated with yield under water limiting conditions. These data lay out a regulatory connection between abiotic stress and fiber yield in cotton that appears conserved in other systems such as Arabidopsis. This regulatory mechanism highlights how sub-genome dynamics contribute to phenotypic stress-response plasticity in cotton.

plant biology↗

Physiological networks governing salinity tolerance potentials in Gossypium hirsutum germplasm

Toxic ions begin to accumulate in tissues of salt-stressed plants after the initial osmotic shock. In glycophytes, the ability to mobilize or sequester excess ions define tolerance mechanisms. Mobilization and sequestration of excess Na+ involves three transport mechanisms facilitated by the plasma membrane H+/Na+ antiporter (SOS1), vacuolar H+/Na+ antiporter (NHX1), and Na+/K+ transporter in vascular tissues (HKT1). While the cultivated Gossypium hirsutum (upland cotton) is significantly more tolerant to salinity relative to other crops, the critical factors contributing to the observed variation for tolerance potential across the germplasm has not been fully scrutinized. In this study, the spatio-temporal patterns of Na+ accumulation at different severities of salt stress were investigated across a minimal comparative panel representing the spectrum of genetic diversity across the improved cotton germplasm. The goal was to define the importance of integrative or network effects relative to the direct effects of Na+ homeostasis mechanisms mediated by GhHKT1, GhSOS1, and GhNHX1. Multi-dimensional physio-morphometric attributes were investigated in univariate and multivariate statistical contexts, as well as the relationship between variables using structural equation modeling. Results showed that mobilized or sequestered Na+ may contribute to the baseline salinity tolerance, but the observed variance in overall tolerance potential across a meaningful subset of the germplasm were more significantly associated to antioxidant capacity, maintenance of stomatal conductance, chlorophyll content, and divalent cations, and other physiological interactions occurring through complex networks. One-Sentence SummaryVariation in salinity tolerance potential across the tetraploid cultivated Gossypium germplasm is better explained by complex physiological networks rather than just cellular Na+ homeostasis.

physiology↗