Literature DB >> 26764377

The LSM1-7 Complex Differentially Regulates Arabidopsis Tolerance to Abiotic Stress Conditions by Promoting Selective mRNA Decapping.

Carlos Perea-Resa1, Cristian Carrasco-López1, Rafael Catalá1, Veronika Turečková2, Ondrej Novak2, Weiping Zhang3, Leslie Sieburth3, José Manuel Jiménez-Gómez4, Julio Salinas5.   

Abstract

In eukaryotes, the decapping machinery is highly conserved and plays an essential role in controlling mRNA stability, a key step in the regulation of gene expression. Yet, the role of mRNA decapping in shaping gene expression profiles in response to environmental cues and the operating molecular mechanisms are poorly understood. Here, we provide genetic and molecular evidence that a component of the decapping machinery, the LSM1-7 complex, plays a critical role in plant tolerance to abiotic stresses. Our results demonstrate that, depending on the stress, the complex from Arabidopsis thaliana interacts with different selected stress-inducible transcripts targeting them for decapping and subsequent degradation. This interaction ensures the correct turnover of the target transcripts and, consequently, the appropriate patterns of downstream stress-responsive gene expression that are required for plant adaptation. Remarkably, among the selected target transcripts of the LSM1-7 complex are those encoding NCED3 and NCED5, two key enzymes in abscisic acid (ABA) biosynthesis. We demonstrate that the complex modulates ABA levels in Arabidopsis exposed to cold and high salt by differentially controlling NCED3 and NCED5 mRNA turnover, which represents a new layer of regulation in ABA biosynthesis in response to abiotic stress. Our findings uncover an unanticipated functional plasticity of the mRNA decapping machinery to modulate the relationship between plants and their environment.
© 2016 American Society of Plant Biologists. All rights reserved.

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Year:  2016        PMID: 26764377      PMCID: PMC4790874          DOI: 10.1105/tpc.15.00867

Source DB:  PubMed          Journal:  Plant Cell        ISSN: 1040-4651            Impact factor:   11.277


  45 in total

1.  Plant stress granules and mRNA processing bodies are distinct from heat stress granules.

Authors:  Christian Weber; Lutz Nover; Markus Fauth
Journal:  Plant J       Date:  2008-08-06       Impact factor: 6.417

2.  A gene regulatory network controlled by the NAC transcription factor ANAC092/AtNAC2/ORE1 during salt-promoted senescence.

Authors:  Salma Balazadeh; Hamad Siddiqui; Annapurna D Allu; Lilian P Matallana-Ramirez; Camila Caldana; Mohammad Mehrnia; Maria-Inés Zanor; Barbara Köhler; Bernd Mueller-Roeber
Journal:  Plant J       Date:  2010-01-22       Impact factor: 6.417

3.  Diffuse decapping enzyme DCP2 accumulates in DCP1 foci under heat stress in Arabidopsis thaliana.

Authors:  Kazuki Motomura; Quy T N Le; Takahiro Hamada; Natsumaro Kutsuna; Shoji Mano; Mikio Nishimura; Yuichiro Watanabe
Journal:  Plant Cell Physiol       Date:  2014-10-22       Impact factor: 4.927

4.  Activated expression of WRKY57 confers drought tolerance in Arabidopsis.

Authors:  Yanjuan Jiang; Gang Liang; Diqiu Yu
Journal:  Mol Plant       Date:  2012-08-28       Impact factor: 13.164

5.  Arabidopsis histidine kinase 5 regulates salt sensitivity and resistance against bacterial and fungal infection.

Authors:  Jasmine Pham; Jasmine Liu; Mark H Bennett; John W Mansfield; Radhika Desikan
Journal:  New Phytol       Date:  2012-01-18       Impact factor: 10.151

6.  LSM proteins provide accurate splicing and decay of selected transcripts to ensure normal Arabidopsis development.

Authors:  Carlos Perea-Resa; Tamara Hernández-Verdeja; Rosa López-Cobollo; María del Mar Castellano; Julio Salinas
Journal:  Plant Cell       Date:  2012-12-07       Impact factor: 11.277

7.  Arabidopsis decapping 5 is required for mRNA decapping, P-body formation, and translational repression during postembryonic development.

Authors:  Jun Xu; Nam-Hai Chua
Journal:  Plant Cell       Date:  2009-10-23       Impact factor: 11.277

Review 8.  RNA degradation in Saccharomyces cerevisae.

Authors:  Roy Parker
Journal:  Genetics       Date:  2012-07       Impact factor: 4.562

9.  Cold signaling and cold response in plants.

Authors:  Kenji Miura; Tsuyoshi Furumoto
Journal:  Int J Mol Sci       Date:  2013-03-06       Impact factor: 5.923

10.  An hnRNP-like RNA-binding protein affects alternative splicing by in vivo interaction with transcripts in Arabidopsis thaliana.

Authors:  Corinna Streitner; Tino Köster; Craig G Simpson; Paul Shaw; Selahattin Danisman; John W S Brown; Dorothee Staiger
Journal:  Nucleic Acids Res       Date:  2012-10-04       Impact factor: 16.971

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  19 in total

1.  A GmSIN1/GmNCED3s/GmRbohBs Feed-Forward Loop Acts as a Signal Amplifier That Regulates Root Growth in Soybean Exposed to Salt Stress.

Authors:  Shuo Li; Nan Wang; Dandan Ji; Wenxiao Zhang; Ying Wang; Yanchong Yu; Shizhen Zhao; Menghua Lyu; Juanjuan You; Yangyang Zhang; Luli Wang; Xiaofang Wang; Zhenhua Liu; Jianhua Tong; Langtao Xiao; Ming-Yi Bai; Fengning Xiang
Journal:  Plant Cell       Date:  2019-06-21       Impact factor: 11.277

Review 2.  Interconnections between mRNA degradation and RDR-dependent siRNA production in mRNA turnover in plants.

Authors:  Masayuki Tsuzuki; Kazuki Motomura; Naoyoshi Kumakura; Atsushi Takeda
Journal:  J Plant Res       Date:  2017-02-14       Impact factor: 2.629

3.  HSP101 Interacts with the Proteasome and Promotes the Clearance of Ubiquitylated Protein Aggregates.

Authors:  Fionn McLoughlin; Minsoo Kim; Richard S Marshall; Richard D Vierstra; Elizabeth Vierling
Journal:  Plant Physiol       Date:  2019-05-21       Impact factor: 8.340

4.  DHH1/DDX6-like RNA helicases maintain ephemeral half-lives of stress-response mRNAs.

Authors:  Thanin Chantarachot; Reed S Sorenson; Maureen Hummel; Haiyan Ke; Alek T Kettenburg; Daniel Chen; Karen Aiyetiwa; Katayoon Dehesh; Thomas Eulgem; Leslie E Sieburth; Julia Bailey-Serres
Journal:  Nat Plants       Date:  2020-06-01       Impact factor: 15.793

Review 5.  Polysomes, Stress Granules, and Processing Bodies: A Dynamic Triumvirate Controlling Cytoplasmic mRNA Fate and Function.

Authors:  Thanin Chantarachot; Julia Bailey-Serres
Journal:  Plant Physiol       Date:  2017-11-20       Impact factor: 8.340

6.  SnRK2 Protein Kinases and mRNA Decapping Machinery Control Root Development and Response to Salt.

Authors:  Dorota Kawa; A Jessica Meyer; Henk L Dekker; Ahmed M Abd-El-Haliem; Kris Gevaert; Eveline Van De Slijke; Justyna Maszkowska; Maria Bucholc; Grażyna Dobrowolska; Geert De Jaeger; Robert C Schuurink; Michel A Haring; Christa Testerink
Journal:  Plant Physiol       Date:  2019-09-30       Impact factor: 8.340

7.  Environment-dependent regulation of spliceosome activity by the LSM2-8 complex in Arabidopsis.

Authors:  Cristian Carrasco-López; Tamara Hernández-Verdeja; Carlos Perea-Resa; David Abia; Rafael Catalá; Julio Salinas
Journal:  Nucleic Acids Res       Date:  2017-07-07       Impact factor: 16.971

8.  Heat Shock Protein HSP101 Affects the Release of Ribosomal Protein mRNAs for Recovery after Heat Shock.

Authors:  Rémy Merret; Marie-Christine Carpentier; Jean-Jacques Favory; Claire Picart; Julie Descombin; Cécile Bousquet-Antonelli; Pascal Tillard; Laurence Lejay; Jean-Marc Deragon; Yee-Yung Charng
Journal:  Plant Physiol       Date:  2017-04-05       Impact factor: 8.340

9.  Orchestration of Processing Body Dynamics and mRNA Decay in Arabidopsis Immunity.

Authors:  Xiao Yu; Bo Li; Geng-Jen Jang; Shan Jiang; Daohong Jiang; Jyan-Chyun Jang; Shu-Hsing Wu; Libo Shan; Ping He
Journal:  Cell Rep       Date:  2019-08-20       Impact factor: 9.423

10.  Arabidopsis mRNA decay landscape arises from specialized RNA decay substrates, decapping-mediated feedback, and redundancy.

Authors:  Reed S Sorenson; Malia J Deshotel; Katrina Johnson; Frederick R Adler; Leslie E Sieburth
Journal:  Proc Natl Acad Sci U S A       Date:  2018-01-31       Impact factor: 11.205

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