Cargando…
Global transcriptome analysis of two ameiotic1 alleles in maize anthers: defining steps in meiotic entry and progression through prophase I
BACKGROUND: Developmental cues to start meiosis occur late in plants. Ameiotic1 (Am1) encodes a plant-specific nuclear protein (AM1) required for meiotic entry and progression through early prophase I. Pollen mother cells (PMCs) remain mitotic in most am1 mutants including am1-489, while am1-praI pe...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180651/ https://www.ncbi.nlm.nih.gov/pubmed/21867558 http://dx.doi.org/10.1186/1471-2229-11-120 |
_version_ | 1782212671015223296 |
---|---|
author | Nan, Guo-Ling Ronceret, Arnaud Wang, Rachel C Fernandes, John F Cande, W Zacheus Walbot, Virginia |
author_facet | Nan, Guo-Ling Ronceret, Arnaud Wang, Rachel C Fernandes, John F Cande, W Zacheus Walbot, Virginia |
author_sort | Nan, Guo-Ling |
collection | PubMed |
description | BACKGROUND: Developmental cues to start meiosis occur late in plants. Ameiotic1 (Am1) encodes a plant-specific nuclear protein (AM1) required for meiotic entry and progression through early prophase I. Pollen mother cells (PMCs) remain mitotic in most am1 mutants including am1-489, while am1-praI permits meiotic entry but PMCs arrest at the leptotene/zygotene (L/Z) transition, defining the roles of AM1 protein in two distinct steps of meiosis. To gain more insights into the roles of AM1 in the transcriptional pre-meiotic and meiotic programs, we report here an in depth analysis of gene expression alterations in carefully staged anthers at 1 mm (meiotic entry) and 1.5 mm (L/Z) caused by each of these am1 alleles. RESULTS: 1.0 mm and 1.5 mm anthers of am1-489 and am1-praI were profiled in comparison to fertile siblings on Agilent(® )4 × 44 K microarrays. Both am1-489 and am1-praI anthers are cytologically normal at 1.0 mm and show moderate transcriptome alterations. At the 1.5-mm stage both mutants are aberrant cytologically, and show more drastic transcriptome changes. There are substantially more absolute On/Off and twice as many differentially expressed genes (sterile versus fertile) in am1-489 than in am1-praI. At 1.5 mm a total of 4,418 genes are up- or down-regulated in either am1-489 or am1-praI anthers. These are predominantly stage-specific transcripts. Many putative meiosis-related genes were found among them including a small subset of allele-specific, mis-regulated genes specific to the PMCs. Nearly 60% of transcriptome changes in the set of transcripts mis-regulated in both mutants (N = 530) are enriched in PMCs, and only 1% are enriched in the tapetal cell transcriptome. All array data reported herein will be deposited and accessible at MaizeGDB http://www.maizegdb.org/. CONCLUSIONS: Our analysis of anther transcriptome modulations by two distinct am1 alleles, am1-489 and am1-praI, redefines the role of AM1 as a modulator of expression of a subset of meiotic genes, important for meiotic progression and provided stage-specific insights into the genetic networks associated with meiotic entry and early prophase I progression. |
format | Online Article Text |
id | pubmed-3180651 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31806512011-09-27 Global transcriptome analysis of two ameiotic1 alleles in maize anthers: defining steps in meiotic entry and progression through prophase I Nan, Guo-Ling Ronceret, Arnaud Wang, Rachel C Fernandes, John F Cande, W Zacheus Walbot, Virginia BMC Plant Biol Research Article BACKGROUND: Developmental cues to start meiosis occur late in plants. Ameiotic1 (Am1) encodes a plant-specific nuclear protein (AM1) required for meiotic entry and progression through early prophase I. Pollen mother cells (PMCs) remain mitotic in most am1 mutants including am1-489, while am1-praI permits meiotic entry but PMCs arrest at the leptotene/zygotene (L/Z) transition, defining the roles of AM1 protein in two distinct steps of meiosis. To gain more insights into the roles of AM1 in the transcriptional pre-meiotic and meiotic programs, we report here an in depth analysis of gene expression alterations in carefully staged anthers at 1 mm (meiotic entry) and 1.5 mm (L/Z) caused by each of these am1 alleles. RESULTS: 1.0 mm and 1.5 mm anthers of am1-489 and am1-praI were profiled in comparison to fertile siblings on Agilent(® )4 × 44 K microarrays. Both am1-489 and am1-praI anthers are cytologically normal at 1.0 mm and show moderate transcriptome alterations. At the 1.5-mm stage both mutants are aberrant cytologically, and show more drastic transcriptome changes. There are substantially more absolute On/Off and twice as many differentially expressed genes (sterile versus fertile) in am1-489 than in am1-praI. At 1.5 mm a total of 4,418 genes are up- or down-regulated in either am1-489 or am1-praI anthers. These are predominantly stage-specific transcripts. Many putative meiosis-related genes were found among them including a small subset of allele-specific, mis-regulated genes specific to the PMCs. Nearly 60% of transcriptome changes in the set of transcripts mis-regulated in both mutants (N = 530) are enriched in PMCs, and only 1% are enriched in the tapetal cell transcriptome. All array data reported herein will be deposited and accessible at MaizeGDB http://www.maizegdb.org/. CONCLUSIONS: Our analysis of anther transcriptome modulations by two distinct am1 alleles, am1-489 and am1-praI, redefines the role of AM1 as a modulator of expression of a subset of meiotic genes, important for meiotic progression and provided stage-specific insights into the genetic networks associated with meiotic entry and early prophase I progression. BioMed Central 2011-08-26 /pmc/articles/PMC3180651/ /pubmed/21867558 http://dx.doi.org/10.1186/1471-2229-11-120 Text en Copyright ©2011 Nan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Nan, Guo-Ling Ronceret, Arnaud Wang, Rachel C Fernandes, John F Cande, W Zacheus Walbot, Virginia Global transcriptome analysis of two ameiotic1 alleles in maize anthers: defining steps in meiotic entry and progression through prophase I |
title | Global transcriptome analysis of two ameiotic1 alleles in maize anthers: defining steps in meiotic entry and progression through prophase I |
title_full | Global transcriptome analysis of two ameiotic1 alleles in maize anthers: defining steps in meiotic entry and progression through prophase I |
title_fullStr | Global transcriptome analysis of two ameiotic1 alleles in maize anthers: defining steps in meiotic entry and progression through prophase I |
title_full_unstemmed | Global transcriptome analysis of two ameiotic1 alleles in maize anthers: defining steps in meiotic entry and progression through prophase I |
title_short | Global transcriptome analysis of two ameiotic1 alleles in maize anthers: defining steps in meiotic entry and progression through prophase I |
title_sort | global transcriptome analysis of two ameiotic1 alleles in maize anthers: defining steps in meiotic entry and progression through prophase i |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180651/ https://www.ncbi.nlm.nih.gov/pubmed/21867558 http://dx.doi.org/10.1186/1471-2229-11-120 |
work_keys_str_mv | AT nanguoling globaltranscriptomeanalysisoftwoameiotic1allelesinmaizeanthersdefiningstepsinmeioticentryandprogressionthroughprophasei AT ronceretarnaud globaltranscriptomeanalysisoftwoameiotic1allelesinmaizeanthersdefiningstepsinmeioticentryandprogressionthroughprophasei AT wangrachelc globaltranscriptomeanalysisoftwoameiotic1allelesinmaizeanthersdefiningstepsinmeioticentryandprogressionthroughprophasei AT fernandesjohnf globaltranscriptomeanalysisoftwoameiotic1allelesinmaizeanthersdefiningstepsinmeioticentryandprogressionthroughprophasei AT candewzacheus globaltranscriptomeanalysisoftwoameiotic1allelesinmaizeanthersdefiningstepsinmeioticentryandprogressionthroughprophasei AT walbotvirginia globaltranscriptomeanalysisoftwoameiotic1allelesinmaizeanthersdefiningstepsinmeioticentryandprogressionthroughprophasei |