Publications by authors named "Kumari Billakurthi"

C species have evolved more than 60 times independently from C ancestors. This multiple and parallel evolution of the complex C trait suggests common underlying evolutionary mechanisms, which could be identified by comparative analysis of closely related C and C species. Efficient C function depends on a distinctive leaf anatomy that is characterised by enlarged, chloroplast-rich bundle sheath cells and narrow vein spacing.

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Chloroplasts develop from undifferentiated plastids in response to light. In angiosperms, after the perception of light, the Elongated Hypocotyl 5 (HY5) transcription factor initiates photomorphogenesis, and two families of transcription factors known as GOLDEN2-LIKE (GLK) and GATA are considered master regulators of chloroplast development. In addition, the MIR171-targeted SCARECROW-LIKE GRAS transcription factors also impact chlorophyll biosynthesis.

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Chloroplast biogenesis is dependent on master regulators from the GOLDEN2-LIKE (GLK) family of transcription factors. However, glk mutants contain residual chlorophyll, indicating that other proteins must be involved. Here, we identify MYB-related transcription factors as regulators of chloroplast biogenesis in the liverwort Marchantia polymorpha and angiosperm Arabidopsis thaliana.

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Background: It has been proposed that engineering the C photosynthetic pathway into C crops could significantly increase yield. This goal requires an increase in the chloroplast compartment of bundle sheath cells in C species. To facilitate large-scale testing of candidate regulators of chloroplast development in the rice bundle sheath, a simple and robust method to phenotype this tissue in C species is required.

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A key feature of C Kranz anatomy is the presence of an enlarged, photosynthetically highly active bundle sheath whose cells contain large numbers of chloroplasts. With the aim to identify novel candidate regulators of C bundle sheath development, we performed an activation tagging screen with . The reporter gene used encoded a chloroplast-targeted GFP protein preferentially expressed in the bundle sheath, and the promoter of the C phosphopyruvate carboxylase gene from served as activation tag because of its activity in all chlorenchymatous tissues of .

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This article comments on: . 2020. BIOMASS YIELD 1 regulates Sorghum biomass and grain yield via the shikimate pathway.

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The evolution of C photosynthesis proceeded stepwise with each small step increasing the fitness of the plant. An important pre-condition for the introduction of a functional C cycle is the photosynthetic activation of the C bundle sheath by increasing its volume and organelle number. Therefore, to engineer C photosynthesis into existing C crops, information about genes that control the bundle sheath cell size and organelle content is needed.

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C photosynthesis is a carbon-concentrating mechanism that evolved independently more than 60 times in a wide range of angiosperm lineages. Among other alterations, the evolution of C from ancestral C photosynthesis requires changes in the expression of a vast number of genes. Differential gene expression analyses between closely related C and C species have significantly increased our understanding of C functioning and evolution.

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Some species of Salsoleae (Chenopodiaceae) convert from C photosynthesis during the seedling stage to the C pathway in adult leaves. This unique developmental transition of photosynthetic pathways offers the exceptional opportunity to follow the development of the derived C syndrome from the C condition within individual plants, avoiding phylogenetic noise. Here we investigate Salsola soda, a little-studied species from tribe Salsoleae, using an ontogenetic approach.

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