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Johal, G.

Publications and source records attributed to Johal, G..

3 recordsLinked to original sources

Variation in maize chlorophyll biosynthesis alters plant architecture

Chlorophyll is a tetrapyrrole metabolite essential for photosynthesis in plants. The oil yellow1 (oy1) gene of maize encodes subunit I of Magnesium chelatase, the enzyme catalyzing the first committed step of chlorophyll biosynthesis. A range of chlorophyll contents and net CO2 assimilation rates can be achieved in maize by combining a semi-dominant mutant allele, Oy1-N1989, and cis-regulatory alleles encoded by the Mo17 inbred called very oil yellow1 (vey1). We previously demonstrated that these allelic interactions can delay reproductive maturity. In this study, we demonstrate that multiple gross morphological traits respond to a reduction in chlorophyll. We found that stalk width, number of lateral branches (tillers), and branching of the inflorescence decline with a decrease in chlorophyll level. Chlorophyll variation suppressed tillering in multiple maize mutants including teosinte branched1, grassy tiller1, and Tillering1 as well as the tiller number1 QTL responsible for tillering in many sweet corn varieties. In contrast to these traits, plant height showed a non-linear response to chlorophyll levels. Weak suppression of Oy1-N1989 by vey1B73 resulted in a significant increase in mutant plant height. This was true in multiple mapping populations, isogenic inbreds, and hybrid backgrounds. Enhancement of the Oy1-N1989 mutants by the vey1Mo17 allele reduced chlorophyll contents and plant height in mapping populations and isogenic inbred background. We demonstrate that the effects of reduced chlorophyll content on plant growth and development are complex and that the genetic relationship depends on the trait. We propose that growth control for branching and architecture are downstream of energy balance sensing.

plant biology↗

Interaction between induced and natural variation at oil yellow1 delays flowering in maize

We previously demonstrated that maize (Zea mays) locus very oil yellow1 (vey1) encodes a putative cis-regulatory expression polymorphism at the magnesium chelatase subunit I gene (aka oil yellow1) that strongly modifies the chlorophyll content of the semi-dominant Oy1-N1989 mutants. The vey1 allele of Mo17 inbred line reduces chlorophyll content in the mutants leading to reduced photosynthetic output. Oy1-N1989 mutants in B73 reached reproductive maturity four days later than wild-type siblings. Enhancement of Oy1-N1989 by the Mo17 allele at the vey1 QTL delayed maturity further, resulting in detection of a flowering time QTL in two bi-parental mapping populations crossed to Oy1-N1989. The near isogenic lines of B73 harboring the vey1 allele from Mo17 delayed flowering of Oy1-N1989 mutants by twelve days. Just as previously observed for chlorophyll content, vey1 had no effect on reproductive maturity in the absence of the Oy1-N1989 allele. Loss of chlorophyll biosynthesis in Oy1-N1989 mutants and enhancement by vey1 reduced CO2 assimilation. We attempted to separate the effects of photosynthesis on the induction of flowering from a possible impact of chlorophyll metabolites and retrograde signaling by manually reducing leaf area. Removal of leaves, independent of the Oy1-N1989 mutant, delayed flowering but surprisingly reduced chlorophyll contents of emerging leaves. Thus, defoliation did not completely separate the identity of the signal(s) that regulates flowering time from changes in chlorophyll content in the foliage. These findings illustrate the necessity to explore the linkage between metabolism and the mechanisms that connect it to flowering time regulation.

plant biology↗

Phytohormone Inhibitor Treatments Phenocopy Brassinosteroid And Gibberellin Dwarf Mutant Interactions In Maize

Phytohormone biosynthesis produces metabolites with profound effects on plant growth and development. Modulation of hormone levels during developmental events, in response to the environment, by genetic polymorphism, or by chemical application can reveal the plant processes most responsive to a phytohormone. In many cases, chemical inhibitors are applied and the levels of specific phytohormones are measured to determine if, and which, phytohormone is affected by a molecule. In many cases, the sensitivity of biochemical testing has determined multiple pathways affected by a single inhibitor. Genetic studies are not subject to this problem, and a wealth of data about the morphological impacts of hormone biosynthetic inhibition has accumulated through the study of enzyme mutants. We previously identified a complex interplay between brassinosteroid (BR) and gibberellin (GA) in maize, where the interdependence of the two differs dependent on the developmental context. We found that: GA is required for loss of BR to induce retained pistils in the tassel florets (POPIT); BR is required for the loss of GA to induce tiller outgrowth; BR and GA are additive for plant height; BR has no effect on the induction of anther retention in ear florets of GA mutants. In this work, we sought to assess the specificity of three triazole inhibitors of cytochrome P450s by determining their abilities to recapitulate the phenotype of double mutants. The GA biosynthetic inhibitors uniconazole (UCZ) and paclobutrazol (PAC) were applied to the BR biosynthetic mutant na2 and all double mutant phenotypes were recovered in the UCZ treatment. PAC was unable to suppress the retention of pistils in the tassels of nana plant2 (na2) mutant plants. The BR biosynthetic inhibitor propiconazole (PCZ) suppressed tiller outgrowth in the GA biosynthetic mutant dwarf5 (d5). All treatments were additive with genetic mutants for effects on plant height. Due to additional measurements done here but not in previous studies of the double mutants, we detected new interactions between GA and BR biosynthesis affecting plastochron index and tassel branching. These experiments, a refinement of our previous model, and a discussion of the extension of this type of work are presented.

plant biology↗