Literature DB >> 27872247

Two Membrane-Anchored Aspartic Proteases Contribute to Pollen and Ovule Development.

Hui Gao1,2, Yinghui Zhang1,2, Wanlei Wang1,2, Keke Zhao1,2, Chunmei Liu1,2, Lin Bai1,2, Rui Li3,4, Yi Guo3,4.   

Abstract

Aspartic proteases are a class of proteolytic enzymes with conserved aspartate residues, which are implicated in protein processing, maturation, and degradation. Compared with yeast and animals, plants possess a larger aspartic protease family. However, little is known about most of these enzymes. Here, we characterized two Arabidopsis (Arabidopsis thaliana) putative glycosylphosphatidylinositol (GPI)-anchored aspartic protease genes, A36 and A39, which are highly expressed in pollen and pollen tubes. a36 and a36 a39 mutants display significantly reduced pollen activity. Transmission electron microscopy and terminal-deoxynucleotidyl transferase-mediated nick end labeling assays further revealed that the unviable pollen in a36 a39 may undergo unanticipated apoptosis-like programmed cell death. The degeneration of female gametes also occurred in a36 a39 Aniline Blue staining, scanning electron microscopy, and semi in vitro guidance assays indicated that the micropylar guidance of pollen tubes is significantly compromised in a36 a39 A36 and A39 that were fused with green fluorescent protein are localized to the plasma membrane and display punctate cytosolic localization and colocalize with the GPI-anchored protein COBRA-LIKE10. Furthermore, in a36 a39, the abundance of highly methylesterified homogalacturonans and xyloglucans was increased significantly in the apical pollen tube wall. These results indicate that A36 and A39, two putative GPI-anchored aspartic proteases, play important roles in plant reproduction in Arabidopsis.
© 2017 American Society of Plant Biologists. All Rights Reserved.

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Year:  2016        PMID: 27872247      PMCID: PMC5210706          DOI: 10.1104/pp.16.01719

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  72 in total

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3.  Glycosylphosphatidylinositol anchoring: control through modification.

Authors:  Alice Y Cheung; Chao Li; Yan-jiao Zou; Hen-Ming Wu
Journal:  Plant Physiol       Date:  2014-10       Impact factor: 8.340

Review 4.  Reactive oxygen species as signals that modulate plant stress responses and programmed cell death.

Authors:  Tsanko S Gechev; Frank Van Breusegem; Julie M Stone; Iliya Denev; Christophe Laloi
Journal:  Bioessays       Date:  2006-11       Impact factor: 4.345

5.  Evaluation of pollen viability by enzymatically induced fluorescence; intracellular hydrolysis of fluorescein diacetate.

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Review 6.  Redox regulation in plant programmed cell death.

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Journal:  Plant Cell Environ       Date:  2011-07-25       Impact factor: 7.228

7.  Proteomic analyses of apoplastic proteins from germinating Arabidopsis thaliana pollen.

Authors:  Weina Ge; Yun Song; Cuijun Zhang; Yafang Zhang; Alma L Burlingame; Yi Guo
Journal:  Biochim Biophys Acta       Date:  2011-07-23

8.  Arabidopsis COBRA-LIKE 10, a GPI-anchored protein, mediates directional growth of pollen tubes.

Authors:  Sha Li; Fu-Rong Ge; Ming Xu; Xin-Ying Zhao; Guo-Qiang Huang; Liang-Zi Zhou; Jia-Gang Wang; Anja Kombrink; Sheila McCormick; Xian Sheng Zhang; Yan Zhang
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Review 9.  Hydrogen peroxide as a signal controlling plant programmed cell death.

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Journal:  Oncotarget       Date:  2015-09-29
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  20 in total

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6.  Processes Underlying a Reproductive Barrier in indica-japonica Rice Hybrids Revealed by Transcriptome Analysis.

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Journal:  Plant Physiol       Date:  2017-05-08       Impact factor: 8.340

7.  Expression in Escherichia coli, Refolding, and Purification of Plant Aspartic Proteases.

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Journal:  Methods Mol Biol       Date:  2022

Review 8.  Bridging the GAPs in plant reproduction: a comparison of plant and animal GPI-anchored proteins.

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Journal:  Plant Reprod       Date:  2020-09-18       Impact factor: 3.767

9.  Interaction between endogenous H2O2 and OsVPE3 in the GA-induced PCD of rice aleurone layers.

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Review 10.  Plant proteases during developmental programmed cell death.

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