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      The long pollen tube journey and in vitro pollen germination of Phalaenopsis orchids

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          Pollen biology in P. aphrodite .

          Abstract

          Orchids have a distinct reproductive program. Pollination triggers ovule development and differentiation within flowers, and fertilization occurs days to months after pollination. It is unclear how pollen tubes travel through the developing ovaries during ovule development and when pollen tubes arrive at the mature embryo sac to achieve fertilization. Here, we report a robust staining protocol to image and record the timing of pollen germination, progressive growth of pollen tubes in ovaries, and arrival of pollen tubes at embryo sacs in Phalaenopsis aphrodite. The pollen germinated and pollen tubes entered the ovary 3 days after pollination. Pollen tubes continued to grow and filled the entire cavity of the ovary as the ovary elongated and ovules developed. Pollen tubes were found to enter the matured embryo sacs at approximately 60–65 days after pollination in an acropetal manner. Moreover, these temporal changes in developmental events such as growth of pollen tubes and fertilization were associated with expression of molecular markers. In addition, we developed an in vitro pollen germination protocol, which is valuable to enable studies on pollen tube guidance and tip growth regulation in Phalaenopsis orchids and possibly in other orchid species.

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          Defensin-like polypeptide LUREs are pollen tube attractants secreted from synergid cells.

          For more than 140 years, pollen tube guidance in flowering plants has been thought to be mediated by chemoattractants derived from target ovules. However, there has been no convincing evidence of any particular molecule being the true attractant that actually controls the navigation of pollen tubes towards ovules. Emerging data indicate that two synergid cells on the side of the egg cell emit a diffusible, species-specific signal to attract the pollen tube at the last step of pollen tube guidance. Here we report that secreted, cysteine-rich polypeptides (CRPs) in a subgroup of defensin-like proteins are attractants derived from the synergid cells. We isolated synergid cells of Torenia fournieri, a unique plant with a protruding embryo sac, to identify transcripts encoding secreted proteins as candidate molecules for the chemoattractant(s). We found two CRPs, abundantly and predominantly expressed in the synergid cell, which are secreted to the surface of the egg apparatus. Moreover, they showed activity in vitro to attract competent pollen tubes of their own species and were named as LUREs. Injection of morpholino antisense oligomers against the LUREs impaired pollen tube attraction, supporting the finding that LUREs are the attractants derived from the synergid cells of T. fournieri.
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            A floral transmitting tissue-specific glycoprotein attracts pollen tubes and stimulates their growth.

            Pollen tubes elongate directionally in the extracellular matrix of pistil tissues to transport the male gametes from the apically located stigma to the basally located ovary for fertilization. The molecular mechanisms underlying directional pollen tube growth in the pistil are poorly understood. We have purified a glycoprotein, TTS, from tobacco stylar transmitting tissue, which supports pollen tube growth between the stigma and the ovary. TTS proteins belong to the arabinogalactan protein family, and they polymerize readily in vitro in a head-to-tail fashion into oligomeric forms. TTS proteins stimulate pollen tube growth in vitro and attract pollen tubes grown in a semi-in vivo culture system. In vivo, the pollen tube growth rate is reduced in transgenic plants that have significantly reduced levels of TTS proteins as a result of either antisense suppression or sense cosuppression. These results identify TTS protein as a pistil component that positively contributes to pollen tube growth.
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              Megagametogenesis in Arabidopsis wild type and the Gf mutant

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                Author and article information

                Contributors
                denseperu@gmail.com
                886-6-5053707 , scfang@gate.sinica.edu.tw
                Journal
                Plant Reprod
                Plant Reprod
                Plant Reproduction
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                2194-7953
                2194-7961
                25 March 2016
                25 March 2016
                2016
                : 29
                : 179-188
                Affiliations
                [ ]Biotechnology Center in Southern Taiwan, Academia Sinica, Tainan, 741 Taiwan
                [ ]Agricultural Biotechnology Research Center, Academia Sinica, Taipei, 115 Taiwan
                Author notes

                Communicated by Noni Franklin-Tong.

                Article
                280
                10.1007/s00497-016-0280-z
                4909812
                27016359
                1662b6ef-b941-4abc-b677-abb29d8f0d83
                © The Author(s) 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 9 December 2015
                : 7 March 2016
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001869, Academia Sinica;
                Award ID: Project #2016CP02
                Award Recipient :
                Categories
                Original Article
                Custom metadata
                © Springer-Verlag Berlin Heidelberg 2016

                phalaenopsis aphrodite,pollen tube,reproductive development,orchid,in vitro germination

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