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Loss of the Arabidopsis thaliana P4-ATPases ALA6 and ALA7 impairs pollen fitness and alters the pollen tube plasma membrane.
McDowell, Stephen C; López-Marqués, Rosa L; Cohen, Taylor; Brown, Elizabeth; Rosenberg, Alexa; Palmgren, Michael G; Harper, Jeffrey F.
Afiliación
  • McDowell SC; Department of Biochemistry and Molecular Biology, University of Nevada Reno, NV, USA.
  • López-Marqués RL; Centre for Membrane Pumps in Cells and Disease, Department of Plant and Environmental Sciences, University of Copenhagen, Danish National Research Foundation Frederiksberg, Denmark.
  • Cohen T; Department of Biochemistry and Molecular Biology, University of Nevada Reno, NV, USA.
  • Brown E; Department of Biochemistry and Molecular Biology, University of Nevada Reno, NV, USA.
  • Rosenberg A; Department of Biochemistry and Molecular Biology, University of Nevada Reno, NV, USA.
  • Palmgren MG; Centre for Membrane Pumps in Cells and Disease, Department of Plant and Environmental Sciences, University of Copenhagen, Danish National Research Foundation Frederiksberg, Denmark.
  • Harper JF; Department of Biochemistry and Molecular Biology, University of Nevada Reno, NV, USA.
Front Plant Sci ; 6: 197, 2015.
Article en En | MEDLINE | ID: mdl-25954280
ABSTRACT
Members of the P4 subfamily of P-type ATPases are thought to create and maintain lipid asymmetry in biological membranes by flipping specific lipids between membrane leaflets. In Arabidopsis, 7 of the 12 Aminophospholipid ATPase (ALA) family members are expressed in pollen. Here we show that double knockout of ALA6 and ALA7 (ala6/7) results in siliques with a ~2-fold reduction in seed set with a high frequency of empty seed positions near the bottom. Seed set was reduced to near zero when plants were grown under a hot/cold temperature stress. Reciprocal crosses indicate that the ala6/7 reproductive deficiencies are due to a defect related to pollen transmission. In-vitro growth assays provide evidence that ala6/7 pollen tubes are short and slow, with ~2-fold reductions in both maximal growth rate and overall length relative to wild-type. Outcrosses show that when ala6/7 pollen are in competition with wild-type pollen, they have a near 0% success rate in fertilizing ovules near the bottom of the pistil, consistent with ala6/7 pollen having short and slow growth defects. The ala6/7 phenotypes were rescued by the expression of either an ALA6-YFP or GFP-ALA6 fusion protein, which showed localization to both the plasma membrane and highly-mobile endomembrane structures. A mass spectrometry analysis of mature pollen grains revealed significant differences between ala6/7 and wild-type, both in the relative abundance of lipid classes and in the average number of double bonds present in acyl side chains. A change in the properties of the ala6/7 plasma membrane was also indicated by a ~10-fold reduction of labeling by lipophilic FM-dyes relative to wild-type. Together, these results indicate that ALA6 and ALA7 provide redundant activities that function to directly or indirectly change the distribution and abundance of lipids in pollen, and support a model in which ALA6 and ALA7 are critical for pollen fitness under normal and temperature-stress conditions.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Front Plant Sci Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Front Plant Sci Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos