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Transporters involved in pH and K(+) homeostasis affect pollen wall formation, male fertility, and embryo development

Flowering plant genomes encode multiple cation/H(+) exchangers (CHXs) whose functions are largely unknown. AtCHX17, AtCHX18, and AtCHX19 are membrane transporters that modulate K(+) and pH homeostasis and are localized in the dynamic endomembrane system. Loss of function reduced seed set, but the pa...

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Autores principales: Padmanaban, Senthilkumar, Czerny, Daniel D, Levin, Kara A, Leydon, Alexander R, Su, Robert T, Maugel, Timothy K, Zou, Yanjiao, Chanroj, Salil, Cheung, Alice Y, Johnson, Mark A, Sze, Heven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853877/
https://www.ncbi.nlm.nih.gov/pubmed/28338823
http://dx.doi.org/10.1093/jxb/erw483
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author Padmanaban, Senthilkumar
Czerny, Daniel D
Levin, Kara A
Leydon, Alexander R
Su, Robert T
Maugel, Timothy K
Zou, Yanjiao
Chanroj, Salil
Cheung, Alice Y
Johnson, Mark A
Sze, Heven
author_facet Padmanaban, Senthilkumar
Czerny, Daniel D
Levin, Kara A
Leydon, Alexander R
Su, Robert T
Maugel, Timothy K
Zou, Yanjiao
Chanroj, Salil
Cheung, Alice Y
Johnson, Mark A
Sze, Heven
author_sort Padmanaban, Senthilkumar
collection PubMed
description Flowering plant genomes encode multiple cation/H(+) exchangers (CHXs) whose functions are largely unknown. AtCHX17, AtCHX18, and AtCHX19 are membrane transporters that modulate K(+) and pH homeostasis and are localized in the dynamic endomembrane system. Loss of function reduced seed set, but the particular phase(s) of reproduction affected was not determined. Pollen tube growth and ovule targeting of chx17chx18chx19 mutant pollen appeared normal, but reciprocal cross experiments indicate a largely male defect. Although triple mutant pollen tubes reach ovules of a wild-type pistil and a synergid cell degenerated, half of those ovules were unfertilized or showed fertilization of the egg or central cell, but not both female gametes. Fertility could be partially compromised by impaired pollen tube and/or sperm function as CHX19 and CHX18 are expressed in the pollen tube and sperm cell, respectively. When fertilization was successful in self-pollinated mutants, early embryo formation was retarded compared with embryos from wild-type ovules receiving mutant pollen. Thus CHX17 and CHX18 proteins may promote embryo development possibly through the endosperm where these genes are expressed. The reticulate pattern of the pollen wall was disorganized in triple mutants, indicating perturbation of wall formation during male gametophyte development. As pH and cation homeostasis mediated by AtCHX17 affect membrane trafficking and cargo delivery, these results suggest that male fertility, sperm function, and embryo development are dependent on proper cargo sorting and secretion that remodel cell walls, plasma membranes, and extracellular factors.
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spelling pubmed-58538772018-07-25 Transporters involved in pH and K(+) homeostasis affect pollen wall formation, male fertility, and embryo development Padmanaban, Senthilkumar Czerny, Daniel D Levin, Kara A Leydon, Alexander R Su, Robert T Maugel, Timothy K Zou, Yanjiao Chanroj, Salil Cheung, Alice Y Johnson, Mark A Sze, Heven J Exp Bot Research Papers Flowering plant genomes encode multiple cation/H(+) exchangers (CHXs) whose functions are largely unknown. AtCHX17, AtCHX18, and AtCHX19 are membrane transporters that modulate K(+) and pH homeostasis and are localized in the dynamic endomembrane system. Loss of function reduced seed set, but the particular phase(s) of reproduction affected was not determined. Pollen tube growth and ovule targeting of chx17chx18chx19 mutant pollen appeared normal, but reciprocal cross experiments indicate a largely male defect. Although triple mutant pollen tubes reach ovules of a wild-type pistil and a synergid cell degenerated, half of those ovules were unfertilized or showed fertilization of the egg or central cell, but not both female gametes. Fertility could be partially compromised by impaired pollen tube and/or sperm function as CHX19 and CHX18 are expressed in the pollen tube and sperm cell, respectively. When fertilization was successful in self-pollinated mutants, early embryo formation was retarded compared with embryos from wild-type ovules receiving mutant pollen. Thus CHX17 and CHX18 proteins may promote embryo development possibly through the endosperm where these genes are expressed. The reticulate pattern of the pollen wall was disorganized in triple mutants, indicating perturbation of wall formation during male gametophyte development. As pH and cation homeostasis mediated by AtCHX17 affect membrane trafficking and cargo delivery, these results suggest that male fertility, sperm function, and embryo development are dependent on proper cargo sorting and secretion that remodel cell walls, plasma membranes, and extracellular factors. Oxford University Press 2017-06-01 2017-02-23 /pmc/articles/PMC5853877/ /pubmed/28338823 http://dx.doi.org/10.1093/jxb/erw483 Text en © The Author 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Padmanaban, Senthilkumar
Czerny, Daniel D
Levin, Kara A
Leydon, Alexander R
Su, Robert T
Maugel, Timothy K
Zou, Yanjiao
Chanroj, Salil
Cheung, Alice Y
Johnson, Mark A
Sze, Heven
Transporters involved in pH and K(+) homeostasis affect pollen wall formation, male fertility, and embryo development
title Transporters involved in pH and K(+) homeostasis affect pollen wall formation, male fertility, and embryo development
title_full Transporters involved in pH and K(+) homeostasis affect pollen wall formation, male fertility, and embryo development
title_fullStr Transporters involved in pH and K(+) homeostasis affect pollen wall formation, male fertility, and embryo development
title_full_unstemmed Transporters involved in pH and K(+) homeostasis affect pollen wall formation, male fertility, and embryo development
title_short Transporters involved in pH and K(+) homeostasis affect pollen wall formation, male fertility, and embryo development
title_sort transporters involved in ph and k(+) homeostasis affect pollen wall formation, male fertility, and embryo development
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853877/
https://www.ncbi.nlm.nih.gov/pubmed/28338823
http://dx.doi.org/10.1093/jxb/erw483
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