Mechanisms for plant adaptation to space environment (BRIC-18-2) - 09.17.14

Overview | Description | Applications | Operations | Results | Publications | Imagery
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The Biological Research in Canisters (BRIC) hardware supports a variety of biological investigations. The BRIC-18-2 investigation uses the model plant Arabidopsis thaliana to understand the regulatory role of a protein named AtIRE1 (a master regulator of transcription in conditions of stress) in adaptation to spaceflight stress.  

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Information Pending



The following content was provided by Federica Brandizzi, Dr., and is maintained in a database by the ISS Program Science Office.

Experiment Details

OpNom

Principal Investigator(s)

  • Federica Brandizzi, Dr., Michigan State University - Plant Research Laboratory, East Lansing, MI, United States

  • Co-Investigator(s)/Collaborator(s)
    Information Pending
    Developer(s)
    Kennedy Space Center, , FL, United States

    Sponsoring Space Agency
    National Aeronautics and Space Administration (NASA)

    Sponsoring Organization
    Human Exploration and Operations Mission Directorate (HEOMD)

    Research Benefits
    Information Pending

    ISS Expedition Duration
    March 2014 - September 2014

    Expeditions Assigned
    39/40

    Previous ISS Missions
    Information Pending

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    Experiment Description

    Research Overview

    • Successful plant growth in closed-loop life support conditions is a difficult challenge for the realization of long-term habitation of spacecraft and other extraterrestrial environments.
    • In these environments plants can undergo stress induced by a number of factors including changes in gravity, radiations, vibration, limited exchange of gases and suboptimal growth conditions.
    • To facilitate plant life in space, it is crucial to acquire a better understanding of the genetic changes in plants that enable adaptation to the spaceflight environment at a transcriptional level.
       

    Description

    Successful plant growth in closed-loop life support conditions is a difficult challenge for the realization of long-term habitation of spacecraft and other extraterrestrial environments. In such environments, plants can undergo stress induced by a number of factors including changes in gravity, radiations, vibration, limited exchange of gases, and suboptimal growth conditions (temperature, light, nutrients). These sources of stress are often associated with reprogramming of gene expression and can cause limited plant growth, development and yield. To facilitate plant life in space, it is crucial to acquire a better understanding of the genetic changes that enable plant cells to respond to spaceflight stress. To do so, one goal of this proposal is to define the underlying mechanisms of plant adaptation to spaceflight environment at a transcriptional level. We have successfully identified a protein named AtIRE1 as a master regulator of transcription in conditions of stress responses to abiotic, biotic stress and to gravity changes in plants. A better understanding of the signaling pathways controlled by atIRE1 are not well defined, especially in conditions of altered gravity. A better understanding of the signaling pathways controlled by AtIRE1 is important to understand how plants can grow in conditions of stress. We will use in-flight and ground resources along with genomics and transcriptomics analyses in the model plant Arabidopsis thaliana to understand the regulartory role of AtIRE1 in adaptation to space flight stress. Development of our research will continue to contribute to the understanding of basic signaling pathways that are inplace to ensure stress survival in hostile environments, thus making possible the design and growth of plants that are resistant to space stress. To contribute further to the successful realization of habitation in space, we also aim to develop plants that can function as bioindicators of stress during in-flight situations. To do so, we will engineer plants with an AtIRE1 substrate that is activated specifically in conditions of stress and that we will adapt to function as a visual stress reporter. The availability of real-time stress bioindicators will provide scientists and astronauts with direct read-outs of stress in the space environment. The results gathered in our research will contribute to NASA’s strategic plans for the realization of long-term habitation of space and planetary surfaces. Because of the conservation of stress sensing and response mechanisms across multicellular organisms, we expect that our results will also have important implications for the general knowledge of stress and in the design of solutions for space stress management in multicellular organisms, including humans.

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    Applications

    Space Applications

    The BRIC-PDFU hardware provides the capability to conduct biological experiments and deliver fluids in one self-contained piece of hardware without the need for a glovebox.  This approach minimizes resources such as volume, mass and crew time. The results gathered in our research will contribute to NASA’s strategic plans for the realization of long-term habitation of space and planetary surfaces.

    Earth Applications

    Because of the conservation of stress sensing and response mechanisms across multicellular organisms, we expect that our results will also have important implications for the general knowledge of stress and in the design of solutions for space stress management in multicellular organisms, including humans.

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    Operations

    Operational Requirements

    Sterilized seeds will be plated and installed into the BRIC canisters.The seeds will be fixed at two intervals, 7 and 14 days after docking. The first canister is fixated  at 7 days and the second canister is fixated at 14 days.  After fixation, the BRIC canisters will be refrigerated at +4 deg. C until post-landing turnover to the PI. Refrigerated samples are planned for return on the same SpaceX mission as launched. 

    Operational Protocols

    7 days after docking, the BRIC-18-2 payload hardware is accessed for fixation.  A rod is removed from the Rod Kit and inserted into the BRIC-PDFU Actuator Tool.  The BRIC-PDFU Actuator Tool is attached to the selected BRIC-PDFU canister lid in position 1 and is used to mechanically force RNA Later or Gluteraldehyde fluid into the Petri dish.  The process is repeated until all the PDFUs are activated in the first canister.  At 14 days after docking, a second fixation period occurs for the remaining experiment in the PDFUs of the second BRIC canister by performing the same Actuator Tool operation.  24 hours after fixation, the BRIC canister must be transferred to the refrigeration of the samples at +4 deg C or less.

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    Results/More Information
    Information Pending

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    Results Publications

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    Ground Based Results Publications

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    ISS Patents

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    Related Publications

      Brandizzi F, Barlowe C.  Organization of the ER-Golgi interface for membrane traffic control. Nature Reviews Molecular Cell Biology. 2013 June; 14(6): 382-392. DOI: 10.1038/nrm3588. PMID: 23698585.

      Chen Y, Aung K, Rolčík J, Walicki K, Friml J, Brandizzi F.  Inter-regulation of the unfolded protein response and auxin signaling. The Plant Journal. 2014 January; 77(1): 97-107. DOI: 10.1111/tpj.12373. PMID: 24180465.

      Chen Y, Brandizzi F.  Analysis of unfolded protein response in Arabidopsis. Methods in Molecular Biology. 2013; 1043: 73-80. DOI: 10.1007/978-1-62703-532-3_8. PMID: 23913037.

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    Imagery