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细胞类型特异性基因表达的综合分析揭示了拟南芥茎尖分生组织中受 REVOLUTA 和 KANADI1 调控的基因。

An integrated analysis of cell-type specific gene expression reveals genes regulated by REVOLUTA and KANADI1 in the Arabidopsis shoot apical meristem.

机构信息

European Molecular Biology Laboratory, Meyerhofstrasse, Heidelberg, Germany.

National Agri-Food Biotechnology Institute, SAS Nagar, Mohali, Punjab, India.

出版信息

PLoS Genet. 2020 Apr 15;16(4):e1008661. doi: 10.1371/journal.pgen.1008661. eCollection 2020 Apr.

DOI:10.1371/journal.pgen.1008661
PMID:32294082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7266345/
Abstract

In the Arabidopsis thaliana shoot apical meristem (SAM) the expression domains of Class III Homeodomain Leucine Zipper (HD-ZIPIII) and KANADI (KAN) genes are separated by a narrow boundary region from which new organs are initiated. Disruption of this boundary through either loss of function or ectopic expression of HD-ZIPIII and KAN causes ectopic or suppression of organ formation respectively, raising the question of how these transcription factors regulate organogenesis at a molecular level. In this study we develop a multi-channel FACS/RNA-seq approach to characterize global patterns of gene expression across the HD-ZIPIII-KAN1 SAM boundary. We then combine FACS, RNA-seq and perturbations of HD-ZIPIII and KAN expression to identify genes that are both responsive to REV and KAN1 and normally expressed in patterns that correlate with REV and KAN1. Our data reveal that a significant number of genes responsive to REV are regulated in opposite ways depending on time after induction, with genes associated with auxin response and synthesis upregulated initially, but later repressed. We also characterize the cell type specific expression patterns of auxin responsive genes and identify a set of genes involved in organogenesis repressed by both REV and KAN1.

摘要

在拟南芥茎尖分生组织(SAM)中,III 类同源域亮氨酸拉链(HD-ZIPIII)和 KANADI(KAN)基因的表达域被一个狭窄的边界区域隔开,新的器官从这个区域开始形成。通过功能丧失或异位表达 HD-ZIPIII 和 KAN 破坏这个边界,分别导致异位或抑制器官形成,这就提出了这些转录因子如何在分子水平上调节器官发生的问题。在这项研究中,我们开发了一种多通道 FACS/RNA-seq 方法来描述跨越 HD-ZIPIII-KAN1 SAM 边界的基因表达的全局模式。然后,我们结合 FACS、RNA-seq 和对 HD-ZIPIII 和 KAN 表达的干扰,来鉴定那些既对 REV 和 KAN1 有反应,又在与 REV 和 KAN1 相关的模式中正常表达的基因。我们的数据表明,大量对 REV 有反应的基因的调控方式取决于诱导后的时间,与生长素反应和合成相关的基因最初上调,但后来被抑制。我们还描述了生长素反应基因的细胞类型特异性表达模式,并鉴定了一组受 REV 和 KAN1 共同抑制的参与器官发生的基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/f945f7779ebe/pgen.1008661.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/2fd69799d2a2/pgen.1008661.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/35d2a3803022/pgen.1008661.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/866c688520b6/pgen.1008661.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/d8c22701b5d5/pgen.1008661.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/f945f7779ebe/pgen.1008661.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/2fd69799d2a2/pgen.1008661.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/35d2a3803022/pgen.1008661.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/866c688520b6/pgen.1008661.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/d8c22701b5d5/pgen.1008661.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef89/7266345/f945f7779ebe/pgen.1008661.g005.jpg

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