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Regulators of early maize leaf development inferred from transcriptomes of laser capture microdissection (LCM)-isolated embryonic leaf cells

The superior photosynthetic efficiency of C(4) leaves over C(3) leaves is owing to their unique Kranz anatomy, in which the vein is surrounded by one layer of bundle sheath (BS) cells and one layer of mesophyll (M) cells. Kranz anatomy development starts from three contiguous ground meristem (GM) ce...

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Autores principales: Liu, Wen-Yu, Yu, Chun-Ping, Chang, Chao-Kang, Chen, Hsiang-June, Li, Meng-Yun, Chen, Yi-Hua, Shiu, Shin-Han, Ku, Maurice S. B., Tu, Shih-Long, Lu, Mei-Yeh Jade, Li, Wen-Hsiung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436337/
https://www.ncbi.nlm.nih.gov/pubmed/36001691
http://dx.doi.org/10.1073/pnas.2208795119
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author Liu, Wen-Yu
Yu, Chun-Ping
Chang, Chao-Kang
Chen, Hsiang-June
Li, Meng-Yun
Chen, Yi-Hua
Shiu, Shin-Han
Ku, Maurice S. B.
Tu, Shih-Long
Lu, Mei-Yeh Jade
Li, Wen-Hsiung
author_facet Liu, Wen-Yu
Yu, Chun-Ping
Chang, Chao-Kang
Chen, Hsiang-June
Li, Meng-Yun
Chen, Yi-Hua
Shiu, Shin-Han
Ku, Maurice S. B.
Tu, Shih-Long
Lu, Mei-Yeh Jade
Li, Wen-Hsiung
author_sort Liu, Wen-Yu
collection PubMed
description The superior photosynthetic efficiency of C(4) leaves over C(3) leaves is owing to their unique Kranz anatomy, in which the vein is surrounded by one layer of bundle sheath (BS) cells and one layer of mesophyll (M) cells. Kranz anatomy development starts from three contiguous ground meristem (GM) cells, but its regulators and underlying molecular mechanism are largely unknown. To identify the regulators, we obtained the transcriptomes of 11 maize embryonic leaf cell types from five stages of pre-Kranz cells starting from median GM cells and six stages of pre-M cells starting from undifferentiated cells. Principal component and clustering analyses of transcriptomic data revealed rapid pre-Kranz cell differentiation in the first two stages but slow differentiation in the last three stages, suggesting early Kranz cell fate determination. In contrast, pre-M cells exhibit a more prolonged transcriptional differentiation process. Differential gene expression and coexpression analyses identified gene coexpression modules, one of which included 3 auxin transporter and 18 transcription factor (TF) genes, including known regulators of Kranz anatomy and/or vascular development. In situ hybridization of 11 TF genes validated their expression in early Kranz development. We determined the binding motifs of 15 TFs, predicted TF target gene relationships among the 18 TF and 3 auxin transporter genes, and validated 67 predictions by electrophoresis mobility shift assay. From these data, we constructed a gene regulatory network for Kranz development. Our study sheds light on the regulation of early maize leaf development and provides candidate leaf development regulators for future study.
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spelling pubmed-94363372023-02-24 Regulators of early maize leaf development inferred from transcriptomes of laser capture microdissection (LCM)-isolated embryonic leaf cells Liu, Wen-Yu Yu, Chun-Ping Chang, Chao-Kang Chen, Hsiang-June Li, Meng-Yun Chen, Yi-Hua Shiu, Shin-Han Ku, Maurice S. B. Tu, Shih-Long Lu, Mei-Yeh Jade Li, Wen-Hsiung Proc Natl Acad Sci U S A Biological Sciences The superior photosynthetic efficiency of C(4) leaves over C(3) leaves is owing to their unique Kranz anatomy, in which the vein is surrounded by one layer of bundle sheath (BS) cells and one layer of mesophyll (M) cells. Kranz anatomy development starts from three contiguous ground meristem (GM) cells, but its regulators and underlying molecular mechanism are largely unknown. To identify the regulators, we obtained the transcriptomes of 11 maize embryonic leaf cell types from five stages of pre-Kranz cells starting from median GM cells and six stages of pre-M cells starting from undifferentiated cells. Principal component and clustering analyses of transcriptomic data revealed rapid pre-Kranz cell differentiation in the first two stages but slow differentiation in the last three stages, suggesting early Kranz cell fate determination. In contrast, pre-M cells exhibit a more prolonged transcriptional differentiation process. Differential gene expression and coexpression analyses identified gene coexpression modules, one of which included 3 auxin transporter and 18 transcription factor (TF) genes, including known regulators of Kranz anatomy and/or vascular development. In situ hybridization of 11 TF genes validated their expression in early Kranz development. We determined the binding motifs of 15 TFs, predicted TF target gene relationships among the 18 TF and 3 auxin transporter genes, and validated 67 predictions by electrophoresis mobility shift assay. From these data, we constructed a gene regulatory network for Kranz development. Our study sheds light on the regulation of early maize leaf development and provides candidate leaf development regulators for future study. National Academy of Sciences 2022-08-24 2022-08-30 /pmc/articles/PMC9436337/ /pubmed/36001691 http://dx.doi.org/10.1073/pnas.2208795119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Liu, Wen-Yu
Yu, Chun-Ping
Chang, Chao-Kang
Chen, Hsiang-June
Li, Meng-Yun
Chen, Yi-Hua
Shiu, Shin-Han
Ku, Maurice S. B.
Tu, Shih-Long
Lu, Mei-Yeh Jade
Li, Wen-Hsiung
Regulators of early maize leaf development inferred from transcriptomes of laser capture microdissection (LCM)-isolated embryonic leaf cells
title Regulators of early maize leaf development inferred from transcriptomes of laser capture microdissection (LCM)-isolated embryonic leaf cells
title_full Regulators of early maize leaf development inferred from transcriptomes of laser capture microdissection (LCM)-isolated embryonic leaf cells
title_fullStr Regulators of early maize leaf development inferred from transcriptomes of laser capture microdissection (LCM)-isolated embryonic leaf cells
title_full_unstemmed Regulators of early maize leaf development inferred from transcriptomes of laser capture microdissection (LCM)-isolated embryonic leaf cells
title_short Regulators of early maize leaf development inferred from transcriptomes of laser capture microdissection (LCM)-isolated embryonic leaf cells
title_sort regulators of early maize leaf development inferred from transcriptomes of laser capture microdissection (lcm)-isolated embryonic leaf cells
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436337/
https://www.ncbi.nlm.nih.gov/pubmed/36001691
http://dx.doi.org/10.1073/pnas.2208795119
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