Cargando…
Transcriptomic profiling identifies differentially expressed genes associated with programmed cell death of nucellar cells in Ginkgo biloba L.
BACKGROUND: Previously, we demonstrated that pollen chamber formation (PCF) in G. biloba ovules was a process of programmed cell death (PCD) within the nucellar cells at the micropylar end. However, the signal triggering the cascades of the programmed events in these nucellar cells remains unexplore...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396491/ https://www.ncbi.nlm.nih.gov/pubmed/30819114 http://dx.doi.org/10.1186/s12870-019-1671-8 |
_version_ | 1783399263545327616 |
---|---|
author | Li, Dahui Wu, Di Li, Shizhou Guo, Ning Gao, Junshan Sun, Xu Cai, Yongping |
author_facet | Li, Dahui Wu, Di Li, Shizhou Guo, Ning Gao, Junshan Sun, Xu Cai, Yongping |
author_sort | Li, Dahui |
collection | PubMed |
description | BACKGROUND: Previously, we demonstrated that pollen chamber formation (PCF) in G. biloba ovules was a process of programmed cell death (PCD) within the nucellar cells at the micropylar end. However, the signal triggering the cascades of the programmed events in these nucellar cells remains unexplored. RESULTS: A transcriptomic strategy was employed to unravel the mechanism underlying the nucellar PCD via the comparative profiles of RNA-seq between pre-PCF and post-PCF ovules. A total of 5599 differentially expressed genes (DEGs) with significance was identified from G. biloba ovules and classified into three main categories of GO annotation, including 17 biological processes, 15 cellular components and 17 molecular functions. KEGG analysis showed that 72 DEGs were enriched in “Plant hormone signal transduction”. Furthermore, 99 DEGs were found to be associated with the PCD process, including the genes involved in ethylene signaling pathway, PCD initiation, and PCD execution. Moreover, calcium-cytochemical localization indicated that calcium could play a role in regulating PCD events within the nucellar cells during pollen chamber formation in G. biloba ovules. CONCLUSIONS: A putative working model, consisting of three overlapping processes, is proposed for the nucellar PCD: at the stage of PCD preparation, ethylene signaling pathway is activated for transcriptional regulation of the downstream targets; subsequently, at the stage of PCD initiation, the upregulated expression of several transcription factors, i.e., NAC, bHLH, MADS-box, and MYB, further promotes the corresponding transcript levels of CYTOCHROME C and CALMODULINs, thereby, leads to the PCD initiation via the calcium-dependent signaling cascade; finally, at the stage of PCD execution, some proteases like metacaspases and vacuolar processing enzyme for hydrolysis, together with the process of autophagy, play roles in the clearance of cellular components. Afterwards, a pollen chamber is generated from the removal of specific nucellar cells in the developing ovule. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-019-1671-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6396491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63964912019-03-13 Transcriptomic profiling identifies differentially expressed genes associated with programmed cell death of nucellar cells in Ginkgo biloba L. Li, Dahui Wu, Di Li, Shizhou Guo, Ning Gao, Junshan Sun, Xu Cai, Yongping BMC Plant Biol Research Article BACKGROUND: Previously, we demonstrated that pollen chamber formation (PCF) in G. biloba ovules was a process of programmed cell death (PCD) within the nucellar cells at the micropylar end. However, the signal triggering the cascades of the programmed events in these nucellar cells remains unexplored. RESULTS: A transcriptomic strategy was employed to unravel the mechanism underlying the nucellar PCD via the comparative profiles of RNA-seq between pre-PCF and post-PCF ovules. A total of 5599 differentially expressed genes (DEGs) with significance was identified from G. biloba ovules and classified into three main categories of GO annotation, including 17 biological processes, 15 cellular components and 17 molecular functions. KEGG analysis showed that 72 DEGs were enriched in “Plant hormone signal transduction”. Furthermore, 99 DEGs were found to be associated with the PCD process, including the genes involved in ethylene signaling pathway, PCD initiation, and PCD execution. Moreover, calcium-cytochemical localization indicated that calcium could play a role in regulating PCD events within the nucellar cells during pollen chamber formation in G. biloba ovules. CONCLUSIONS: A putative working model, consisting of three overlapping processes, is proposed for the nucellar PCD: at the stage of PCD preparation, ethylene signaling pathway is activated for transcriptional regulation of the downstream targets; subsequently, at the stage of PCD initiation, the upregulated expression of several transcription factors, i.e., NAC, bHLH, MADS-box, and MYB, further promotes the corresponding transcript levels of CYTOCHROME C and CALMODULINs, thereby, leads to the PCD initiation via the calcium-dependent signaling cascade; finally, at the stage of PCD execution, some proteases like metacaspases and vacuolar processing enzyme for hydrolysis, together with the process of autophagy, play roles in the clearance of cellular components. Afterwards, a pollen chamber is generated from the removal of specific nucellar cells in the developing ovule. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-019-1671-8) contains supplementary material, which is available to authorized users. BioMed Central 2019-02-28 /pmc/articles/PMC6396491/ /pubmed/30819114 http://dx.doi.org/10.1186/s12870-019-1671-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Li, Dahui Wu, Di Li, Shizhou Guo, Ning Gao, Junshan Sun, Xu Cai, Yongping Transcriptomic profiling identifies differentially expressed genes associated with programmed cell death of nucellar cells in Ginkgo biloba L. |
title | Transcriptomic profiling identifies differentially expressed genes associated with programmed cell death of nucellar cells in Ginkgo biloba L. |
title_full | Transcriptomic profiling identifies differentially expressed genes associated with programmed cell death of nucellar cells in Ginkgo biloba L. |
title_fullStr | Transcriptomic profiling identifies differentially expressed genes associated with programmed cell death of nucellar cells in Ginkgo biloba L. |
title_full_unstemmed | Transcriptomic profiling identifies differentially expressed genes associated with programmed cell death of nucellar cells in Ginkgo biloba L. |
title_short | Transcriptomic profiling identifies differentially expressed genes associated with programmed cell death of nucellar cells in Ginkgo biloba L. |
title_sort | transcriptomic profiling identifies differentially expressed genes associated with programmed cell death of nucellar cells in ginkgo biloba l. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6396491/ https://www.ncbi.nlm.nih.gov/pubmed/30819114 http://dx.doi.org/10.1186/s12870-019-1671-8 |
work_keys_str_mv | AT lidahui transcriptomicprofilingidentifiesdifferentiallyexpressedgenesassociatedwithprogrammedcelldeathofnucellarcellsinginkgobilobal AT wudi transcriptomicprofilingidentifiesdifferentiallyexpressedgenesassociatedwithprogrammedcelldeathofnucellarcellsinginkgobilobal AT lishizhou transcriptomicprofilingidentifiesdifferentiallyexpressedgenesassociatedwithprogrammedcelldeathofnucellarcellsinginkgobilobal AT guoning transcriptomicprofilingidentifiesdifferentiallyexpressedgenesassociatedwithprogrammedcelldeathofnucellarcellsinginkgobilobal AT gaojunshan transcriptomicprofilingidentifiesdifferentiallyexpressedgenesassociatedwithprogrammedcelldeathofnucellarcellsinginkgobilobal AT sunxu transcriptomicprofilingidentifiesdifferentiallyexpressedgenesassociatedwithprogrammedcelldeathofnucellarcellsinginkgobilobal AT caiyongping transcriptomicprofilingidentifiesdifferentiallyexpressedgenesassociatedwithprogrammedcelldeathofnucellarcellsinginkgobilobal |