scholarly journals A MYB Triad Controls Primary and Phenylpropanoid Metabolites for Pollen Coat Patterning

2019 ◽  
Vol 180 (1) ◽  
pp. 87-108 ◽  
Author(s):  
Maor Battat ◽  
Asa Eitan ◽  
Ilana Rogachev ◽  
Kati Hanhineva ◽  
Alisdair Fernie ◽  
...  
Keyword(s):  
Pollen Coat

scholarly journals Modifying the pollen coat protein composition in Brassica

2002 ◽  
Vol 31 (4) ◽  
pp. 477-486 ◽  
Author(s):  
Elizabeth Foster ◽  
Danielle Schneiderman ◽  
Michel Cloutier ◽  
Stephen Gleddie ◽  
Laurian S. Robert
Keyword(s):  
Coat Protein ◽  
Protein Composition ◽  
Pollen Coat ◽  
Pollen Coat Protein

scholarly journals MS1, a direct target of MS188, regulates the expression of key sporophytic pollen coat protein genes in Arabidopsis

2020 ◽  
Vol 71 (16) ◽  
pp. 4877-4889
Author(s):  
Jie-Yang Lu ◽  
Shuang-Xi Xiong ◽  
Wenzhe Yin ◽  
Xiao-Dong Teng ◽  
Yue Lou ◽  
...  
Keyword(s):  
Fluorescent Protein ◽  
Pollen Wall ◽  
Coat Proteins ◽  
Related Family ◽  
Regulatory Cascade ◽  
Pollen Coat ◽  
Green Fluorescent ◽  
High Level ◽  
And Function

Abstract Sporophytic pollen coat proteins (sPCPs) derived from the anther tapetum are deposited into pollen wall cavities and function in pollen–stigma interactions, pollen hydration, and environmental protection. In Arabidopsis, 13 highly abundant proteins have been identified in pollen coat, including seven major glycine-rich proteins GRP14, 16, 17, 18, 19, 20, and GRP–oleosin; two caleosin-related family proteins (AT1G23240 and AT1G23250); three lipase proteins EXL4, EXL5 and EXL6, and ATA27/BGLU20. Here, we show that GRP14, 17, 18, 19, and EXL4 and EXL6 fused with green fluorescent protein (GFP) are translated in the tapetum and then accumulate in the anther locule following tapetum degeneration. The expression of these sPCPs is dependent on two essential tapetum transcription factors, MALE STERILE188 (MS188) and MALE STERILITY 1 (MS1). The majority of sPCP genes are up-regulated within 30 h after MS1 induction and could be restored by MS1 expression driven by the MS188 promoter in ms188, indicating that MS1 is sufficient to activate their expression; however, additional MS1 downstream factors appear to be required for high-level sPCP expression. Our ChIP, in vivo transactivation assay, and EMSA data indicate that MS188 directly activates MS1. Together, these results reveal a regulatory cascade whereby outer pollen wall formation is regulated by MS188 followed by synthesis of sPCPs controlled by MS1.

Tapetum character states: analytical keys for tapetum types and activities

1997 ◽  
Vol 75 (9) ◽  
pp. 1448-1459 ◽  
Author(s):  
E. Pacini
Keyword(s):  
Pollen Development ◽  
Cell Walls ◽  
Pollen Grains ◽  
Cell Types ◽  
Plastid Differentiation ◽  
Pollen Coat ◽  
Tapetal Cells ◽  
Different Types ◽  
Compound Pollen ◽  
Pollen Formation

The different types of tapetum found in the spermatophyta are described, along with associated characters. The characters (taken singly, pairwise, or in multiple combinations) are (i) tapetum types; (ii) cell walls, tapetum types, and loculus; (iii) tapetal cells individually, tapetum types, and loculus; (iv) number of pollen grains enveloped by tapetal cells and type of pollen dispersing unit; (v) cell types and tapetum types; (vi) number of nuclei per cell and tapetum type; (vii) cycles of hyperactivity; (viii) exine formation; (ix) orbicles; (x) peritapetal membrane; (xi) plastid differentiation; (xii) stage of pollen development in which tapetal cells degenerate and type of pollen coat; (xiii) storage vacuoles; (xiv) sporophytic proteins; and (xv) devices of tapetal origin responsible for compound pollen formation and pollination. Examples are given and an analytical key of structural and functional diversity is provided as a helpful approach to the study of the tapetum. Key words: tapetum types, activities, pollen dispersing units.

scholarly journals Genome-Wide Identification and Comparison of Cysteine Proteases in the Pollen Coat and Other Tissues in Maize

2021 ◽  
Vol 12 ◽  
Author(s):  
Yanhua Li ◽  
Liangjie Niu ◽  
Xiaolin Wu ◽  
Claudia Faleri ◽  
Fuju Tai ◽  
...  
Keyword(s):  
Growth And Development ◽  
Cellular Localization ◽  
Expression Patterns ◽  
Sodium Dodecyl ◽  
Cysteine Proteases ◽  
Immunogold Electron Microscopy ◽  
Upstream Sequence ◽  
Maize Pollen ◽  
Genome Wide ◽  
Pollen Coat

Cysteine proteases, belonging to the C1-papain family, play a major role in plant growth and development, senescence, and immunity. There is evidence to suggest that pollen cysteine protease (CP) (ZmCP03) is involved in regulating the anther development and pollen formation in maize. However, there is no report on the genome-wide identification and comparison of CPs in the pollen coat and other tissues in maize. In this study, a total of 38 homologous genes of ZmCP03 in maize were identified. Subsequently, protein motifs, conserved domains, gene structures, and duplication patterns of 39 CPs are analyzed to explore their evolutionary relationship and potential functions. The cis-elements were identified in the upstream sequence of 39 CPs, especially those that are related to regulating growth and development and responding to environmental stresses and hormones. The expression patterns of these genes displayed remarked difference at a tissue or organ level in maize based on the available transcriptome data in the public database. Quantitative reverse transcription PCR (RT-qPCR) analysis showed that ZmCP03 was preferably expressed at a high level in maize pollen. Analyses by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and immunoblot, immunofluorescence and immunogold electron microscopy all validated the cellular localization of ZmCP03 in both the pollen coat and pollen cytoplasm. In addition, 142 CP genes from Arabidopsis (Arabidopsis thaliana), rice (Oryza sativa) and cotton (Gossypium hirsutum), together with 39 maize CPs, were retrieved to analyze their evolution by comparing with orthologous genes. The results suggested that ZmCP03 was relatively conservative and stable during evolution. This study may provide a referential evidence on the function of ZmCP03 in pollen development and germination in maize.

scholarly journals Genomic Organization of the S Locus: Identification and Characterization of Genes in SLG/SRK Region of S9 Haplotype of Brassica campestris (syn. rapa)

Genetics ◽  
1999 ◽  
Vol 153 (1) ◽  
pp. 391-400 ◽  
Author(s):  
Go Suzuki ◽  
Naoko Kai ◽  
Tamaki Hirose ◽  
Kiichi Fukui ◽  
Takeshi Nishio ◽  
...  
Keyword(s):  
Brassica Campestris ◽  
Protein A ◽  
S Locus ◽  
Cysteine Rich Protein ◽  
Pollen Coat ◽  
Genes Encoding ◽  
Gene Rich Region ◽  
Identification And Characterization ◽  
S Locus Glycoprotein

Abstract In Brassica, two self-incompatibility genes, encoding SLG (S locus glycoprotein) and SRK (S-receptor kinase), are located at the S locus and expressed in the stigma. Recent molecular analysis has revealed that the S locus is highly polymorphic and contains several genes, i.e., SLG, SRK, the as-yet-unidentified pollen S gene(s), and other linked genes. In the present study, we searched for expressed sequences in a 76-kb SLG/SRK region of the S9 haplotype of Brassica campestris (syn. rapa) and identified 10 genes in addition to the four previously identified (SLG9, SRK9, SAE1, and SLL2) in this haplotype. This gene density (1 gene/5.4 kb) suggests that the S locus is embedded in a gene-rich region of the genome. The average G + C content in this region is 32.6%. An En/Spm-type transposon-like element was found downstream of SLG9. Among the genes we identified that had not previously been found to be linked to the S locus were genes encoding a small cysteine-rich protein, a J-domain protein, and an antisilencing protein (ASF1) homologue. The small cysteine-rich protein was similar to a pollen coat protein, named PCP-A1, which had previously been shown to bind SLG.

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