4.5 Article

Cellular and transcriptomic analyses reveal two-staged chloroplast biogenesis underpinning photosynthesis build-up in the wheat leaf

Journal

GENOME BIOLOGY
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13059-021-02366-3

Keywords

Wheat; Plastid; Chloroplast; Leaf development

Funding

  1. Japan Society for the Promotion of Science (JSPS) [26712003]
  2. Core Research for Evolutionary Science and Technology (CREST) of the Japan Science and Technology Agency (JST) [JPMJCR16O4]
  3. Government of India's Ministry of Tribal Affairs
  4. Indian Council of Agricultural Research
  5. BBSRC UK Research and Innoivation (UKRI) [BBP0031171]
  6. Royal Holloway research strategy fund
  7. Grants-in-Aid for Scientific Research [26712003] Funding Source: KAKEN

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Using the developmental gradient in bread wheat leaves, a comprehensive gene expression map was generated capturing the entire developmental gradient from meristematic to fully differentiated cells. The study identified two distinct phases of chloroplast development, involving organelle proliferation and establishment of photosynthetic chloroplasts. Known chloroplast gene expression regulators were predicted to have differential involvement across these stages.
Background The developmental gradient in monocot leaves has been exploited to uncover leaf developmental gene expression programs and chloroplast biogenesis processes. However, the relationship between the two is barely understood, which limits the value of transcriptome data to understand the process of chloroplast development. Results Taking advantage of the developmental gradient in the bread wheat leaf, we provide a simultaneous quantitative analysis for the development of mesophyll cells and of chloroplasts as a cellular compartment. This allows us to generate the first biologically-informed gene expression map of this leaf, with the entire developmental gradient from meristematic to fully differentiated cells captured. We show that the first phase of plastid development begins with organelle proliferation, which extends well beyond cell proliferation, and continues with the establishment and then the build-up of the plastid genetic machinery. The second phase is marked by the development of photosynthetic chloroplasts which occupy the available cellular space. Using a network reconstruction algorithm, we predict that known chloroplast gene expression regulators are differentially involved across those developmental stages. Conclusions Our analysis generates both the first wheat leaf transcriptional map and one of the most comprehensive descriptions to date of the developmental history of chloroplasts in higher plants. It reveals functionally distinct plastid and chloroplast development stages, identifies processes occurring in each of them, and highlights our very limited knowledge of the earliest drivers of plastid biogenesis, while providing a basis for their future identification.

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