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Simulated microgravity, Mars gravity, and 2g hypergravity affect cell cycle regulation, ribosome biogenesis, and epigenetics in Arabidopsis cell cultures

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Abstract

Gravity is the only component of Earth environment that remained constant throughout the entire process of biological evolution. However, it is still unclear how gravity affects plant growth and development. In this study, an in vitro cell culture of Arabidopsis thaliana was exposed to different altered gravity conditions, namely simulated reduced gravity (simulated microgravity, simulated Mars gravity) and hypergravity (2g), to study changes in cell proliferation, cell growth, and epigenetics. The effects after 3, 14, and 24-hours of exposure were evaluated. The most relevant alterations were found in the 24-hour treatment, being more significant for simulated reduced gravity than hypergravity. Cell proliferation and growth were uncoupled under simulated reduced gravity, similarly, as found in meristematic cells from seedlings grown in real or simulated microgravity. The distribution of cell cycle phases was changed, as well as the levels and gene transcription of the tested cell cycle regulators. Ribosome biogenesis was decreased, according to levels and gene transcription of nucleolar proteins and the number of inactive nucleoli. Furthermore, we found alterations in the epigenetic modifications of chromatin. These results show that altered gravity effects include a serious disturbance of cell proliferation and growth, which are cellular functions essential for normal plant development.

Original languageEnglish
Article number6424
Number of pages16
JournalScientific Reports
Volume8
Issue number1
DOIs
Publication statusPublished - 23 Apr 2018

Funding

This work is a part of KY PhD dissertation, which has been published by Universidad Complutense de Madrid, Spain, 2014. The skillful technical assistance of Mrs. Mercedes Carnota (CIB-CSIC) with different lab procedures is gratefully acknowledged, as well as the Technical Services of Genomics and Flow Cytometry of CIB-CSIC for the assistance with the RT-PCR procedures and the analysis of flow cytometry data, respectively, and Mr. Alan Dowson for his support at the TEC-MMG LIS lab (ESA-ESTEC). We also thank Dr. Crisanto Gutierrez, at CBM (UAM-CSIC, Spain) and Dr. Julio Sáez-Vásquez (CNRS-University of Perpignan-Via Domitia, France) for generous supply of MM2d cultures and anti-nucleolin antibody, respectively. Finally, a great thankful acknowledgement to Prof. John Z. Kiss (University of North Carolina at Greensboro, USA) for revision and corrections regarding the English language style and the scientific content of the manuscript. This work was supported by the Spanish “Plan Estatal de Investigación Científica y Ténica y de Innovación” of the Ministry of Economy, Industry and Competitiveness [Grant numbers AYA2012–33982 and ESP2015–64323-R, co-funded by ERDF], by a pre-doctoral fellowship to [Kh.Y.K.] from CSIC, Spain [JAE-PreDoc Program, Ref. JAEPre_2010_01894] the ESA-ELIPS Program [ESA SEGMGSPE_Ph1 Project, contract number 4200022650], and ESA support via contract TEC-MMG/2012/263.

FundersFunder number
Comisión Sectorial de Investigación Científica4200022650, JAEPre_2010_01894
Comisión Asesora de Investigación Científica y Técnica
European Regional Development Fund
Ecological Society of AustraliaTEC-MMG/2012/263
Ministerio de Economía, Industria y Competitividad, Gobierno de EspañaAYA2012–33982, ESP2015–64323-R

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