alignment between pin1 polarity and microtubule orientation in the shoot apical meristem reveals a tight coupling between morphogenesis and auxin transport对齐pin1极性和微管取向之间的顶端分生组织形态发生和生长素运输之间的紧密耦合.pdfVIP

alignment between pin1 polarity and microtubule orientation in the shoot apical meristem reveals a tight coupling between morphogenesis and auxin transport对齐pin1极性和微管取向之间的顶端分生组织形态发生和生长素运输之间的紧密耦合.pdf

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alignment between pin1 polarity and microtubule orientation in the shoot apical meristem reveals a tight coupling between morphogenesis and auxin transport对齐pin1极性和微管取向之间的顶端分生组织形态发生和生长素运输之间的紧密耦合

Alignment between PIN1 Polarity and Microtubule Orientation in the Shoot Apical Meristem Reveals a Tight Coupling between Morphogenesis and Auxin Transport 1.¤ 2. 3. 2 1¤ Marcus G. Heisler , Olivier Hamant , Pawel Krupinski , Magalie Uyttewaal , Carolyn Ohno , Henrik ¨ 3 . 2 1 Jonsson * , Jan Traas *, Elliot M. Meyerowitz * ´ 1 Division of Biology, California Institute of Technology, Pasadena, California, United States of America, 2 INRA, CNRS, ENS, Universite de Lyon, Lyon Cedex, France, 3 Computational Biology and Biological Physics Group, Department of Theoretical Physics, Lund University, Lund, Sweden Abstract Morphogenesis during multicellular development is regulated by intercellular signaling molecules as well as by the mechanical properties of individual cells. In particular, normal patterns of organogenesis in plants require coordination between growth direction and growth magnitude. How this is achieved remains unclear. Here we show that in Arabidopsis thaliana, auxin patterning and cellular growth are linked through a correlated pattern of auxin efflux carrier localization and cortical microtubule orientation. Our experiments reveal that both PIN1 localization and microtubule array orientation are likely to respond to a shared upstream regulator that appears to be biomechanical in nature. Lastly, through mathematical modeling we show that such a biophysical coupling could mediate the feedback loop between auxin and its t

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