Abstract

Radish cytoplasmic male sterility (CMS) has been widely used for breeding in Raphanus and Brassica genera. However, the detailed regulation network of the male sterility remains to be determined. Our previous work has shown that the abnormalities in a CMS radish appeared shortly after the tetrad stage when microspores were malformed and the tapetal cells grew abnormally large. In this work, histological analysis shows that anthers are at the tetrad stage when the radish buds are about 1.5 mm in length. Furthermore, a high throughput RNA sequencing technology was employed to characterize the transcriptome of radish buds with length about 1.5 mm from two CMS lines possessing the CMS-inducing orf138 gene and corresponding near-isogenic maintainer lines. A total of 67,140 unigenes were functionally annotated. Functional terms for these genes are significantly enriched in 55 Gene Ontology (GO) groups and 323 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. The transcriptome detected transcripts for 72 out of a total of 79 protein genes encoded in the chloroplast genome from radish. In contrast, the radish mitochondrial genome contains 34 protein genes, but only 16 protein transcripts were detected from the transcriptome. The transcriptome comparison between CMS and near-isogenic maintainer lines revealed 539 differentially expressed genes (DEGs), indicating that the false positive rate for comparative transcriptome profiling was clearly decreased using two groups of CMS/maintainer lines with different nuclear background. The level of 127 transcripts was increased and 412 transcripts were decreased in the CMS lines. No change in levels of transcripts except CMS-inducing orf138 was identified from the mitochondrial and chloroplast genomes. Some DEGs which would be associated with the CMS, encoding MYB and bHLH transcription factors, pentatricopeptide repeat (PPR) proteins, heat shock transcription factors (HSFs) and heat shock proteins (HSPs), are discussed. The transcriptome dataset and comparative analysis will provide an important resource for further understanding anther development, the CMS mechanism and to improve molecular breeding in radish.

Highlights

  • Plant cytoplasmic male sterility (CMS) is a maternally inherited trait preventing the production of functional pollen but maintaining female fertility

  • No histological differences were observed between the CMS line 9802A1 and the corresponding maintainer line 9802B1 in the anther at the tetrad stage when tetrads were enclosed by a thick callose wall in our previous study [29]

  • Since the abortive phenotype for our radish CMS is cytologically observed shortly after the tetrad stage, it remains to be determined whether three differentially expressed genes (DEGs) encoding a C2H2 zinc-finger transcription factor and two WRKYs are involved in early events of the radish CMS

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Summary

Introduction

Plant cytoplasmic male sterility (CMS) is a maternally inherited trait preventing the production of functional pollen but maintaining female fertility. Pollen fertility of the CMS plants can be restored by corresponding nuclear-encoded fertility restorer genes suggesting that CMS is an ideal model system to study nuclear-cytoplasmic gene interaction [5]. Many novel chimeric mitochondrial genes have been identified and are responsible for CMS through a variety of mechanisms (such as urf from maize, pcf from petunia, orf79/orfH79 from rice, orf224/orf222 from rapeseed etc.) [6,7,8,9,10,11]. A new mitochondrial gene, WA352, was found to confer CMS in rice. Orf138/orf125 confers Ogura/Kosena CMS [18,20], and orf463 is likely to be a causative factor for DCGMS CMS [28]. Comparative transcriptome analysis of radish buds from CMS and their maintainer lines was conducted by Illumina sequencing, which might provide assistance for further deep analysis about anther development and CMS in radish

The Floral Bud Size Is Associated with the Microspore Developmental Stage
Validation of the Expression Difference of DEGs
Plant Materials and RNA Extraction
Histological Analysis
RNA Extraction and RNA-Seq
De Novo Assembly and Database Search
Differential Gene Expression
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