QTLs Associated with Crown Root Angle, Stomatal Conductance, and Maturity in Sorghum
Core Ideas QTLs for crown root angle, stomatal conductance, and maturity were identified in two field studies through the construction of a high‐density bin map. The QTL for stomatal conductance was associated with reduced leaf transpiration but not reduced net assimilation rate. Candidate genes are...
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Veröffentlicht in: | The plant genome 2017-07, Vol.10 (2), p.1-12 |
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Sprache: | eng |
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Zusammenfassung: | Core Ideas
QTLs for crown root angle, stomatal conductance, and maturity were identified in two field studies through the construction of a high‐density bin map.
The QTL for stomatal conductance was associated with reduced leaf transpiration but not reduced net assimilation rate.
Candidate genes are proposed based on the physical location of the QTLs and the function of known genes in those locations.
Three factors that directly affect the water inputs in cropping systems are root architecture, length of the growing season, and stomatal conductance to water vapor (gs). Deeper‐rooted cultivars will perform better under water‐limited conditions because they can access water stored deeper in the soil profile. Reduced gs limits transpiration rate (E) and thus throughout the vegetative phase conserves water that may be used during grain filling in water‐limited environments. Additionally, growing early‐maturing varieties in regions that rely on soil‐stored water is a key water management strategy. To further our understanding of the genetic basis underlying root depth, growing season length, and gs we conducted a quantitative trait locus (QTL) study. A QTL for crown root angle (a proxy for root depth) new to sorghum was identified in chromosome 3. For gs, a QTL in chromosome seven was identified. In a follow‐up field study it was determined that the QTL for gs was associated with reduced E but not with net carbon assimilation rate (A) or shoot biomass. No differences in guard‐cell length or stomatal density were observed among the lines, leading to the conclusion that the observed differences in gs must be explained by partial stomatal closure. The well‐studied maturity gene Ma1 was identified in the QTL for maturity. The transgressive segregation of the population was explained by the possible interaction of Ma1 with other loci. Finally, the most probable position of the genes underlying the QTLs and candidate genes were proposed. |
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ISSN: | 1940-3372 1940-3372 |
DOI: | 10.3835/plantgenome2016.04.0038 |