Abstract

Recently, crop breeders have widely adopted a new biotechnology-based process, termed Seed Production Technology (SPT), to produce hybrid varieties. The SPT does not produce nuclear male-sterile lines, and instead utilizes transgenic SPT maintainer lines to pollinate male-sterile plants for propagation of nuclear-recessive male-sterile lines. A late-stage pollen-specific promoter is an essential component of the pollen-inactivating cassette used by the SPT maintainers. While a number of plant pollen-specific promoters have been reported so far, their usefulness in SPT has remained limited. To increase the repertoire of pollen-specific promoters for the maize community, we conducted a comprehensive comparative analysis of transcriptome profiles of mature pollen and mature anthers against other tissue types. We found that maize pollen has much less expressed genes (>1 FPKM) than other tissue types, but the pollen grain has a large set of distinct genes, called pollen-specific genes, which are exclusively or much higher (100 folds) expressed in pollen than other tissue types. Utilizing transcript abundance and correlation coefficient analysis, 1215 mature pollen-specific (MPS) genes and 1009 mature anther-specific (MAS) genes were identified in B73 transcriptome. These two gene sets had similar GO term and KEGG pathway enrichment patterns, indicating that their members share similar functions in the maize reproductive process. Of the genes, 623 were shared between the two sets, called mature anther- and pollen-specific (MAPS) genes, which represent the late-stage pollen-specific genes of the maize genome. Functional annotation analysis of MAPS showed that 447 MAPS genes (71.7% of MAPS) belonged to genes encoding pollen allergen protein. Their 2-kb promoters were analyzed for cis-element enrichment and six well-known pollen-specific cis-elements (AGAAA, TCCACCA, TGTGGTT, [TA]AAAG, AAATGA, and TTTCT) were found highly enriched in the promoters of MAPS. Interestingly, JA-responsive cis-element GCC box (GCCGCC) and ABA-responsive cis-element-coupling element1 (ABRE-CE1, CCACC) were also found enriched in the MAPS promoters, indicating that JA and ABA signaling likely regulate pollen-specific MAPS expression. This study describes a robust and straightforward pipeline to discover pollen-specific promotes from publicly available data while providing maize breeders and the maize industry a number of late-stage (mature) pollen-specific promoters for use in SPT for hybrid breeding and seed production.

Highlights

  • IntroductionPollen arises from the sporogenous cells in the loculi of the anther

  • In flowering plants, pollen arises from the sporogenous cells in the loculi of the anther

  • A Pearson correlation coefficient analysis of transcript abundance in the 23 tissues showed that transcripts of mature pollen have an insignificant correlation with all tissue types analyzed (Figure S1), indicating that mature pollen possesses a unique transcript profile compared with other maize tissues

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Summary

Introduction

Pollen arises from the sporogenous cells in the loculi of the anther. During phase I, the anther primordia undergo a series of prescribed cell divisions to form a young anther This phase includes three early stages of microspores development: archesporial cells (AR), meiocytes (ME), and the quartet stage of microspores (Q). Phase II includes three stages of pollen development: uninucleate microspore (UM), binucleate microspore (BM), and mature pollen (MP) [1] These two phases have been further divided into 14 successive stages using morphological and cellular features viewed under light microscopy [4]. Stages 1–8 make up phase I and stages 9–14 constitute phase II of anther development [4] For cereals such as maize and rice, anther development has been shown to undergo 14 successive stages, similar to Arabidopsis, to produce mature pollen [5,6,7]. By the end of phase IV, i.e., at the anthesis time, the mature pollen grains (trinucleate microspore, TM) are released from the stomia of maize anther

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