Literature DB >> 15247369

Salt cress. A halophyte and cryophyte Arabidopsis relative model system and its applicability to molecular genetic analyses of growth and development of extremophiles.

Günsu Inan1, Quan Zhang, Pinghua Li, Zenglan Wang, Ziyi Cao, Hui Zhang, Changqing Zhang, Tanya M Quist, S Mark Goodwin, Jianhua Zhu, Huazhong Shi, Barbara Damsz, Tarif Charbaji, Qingqiu Gong, Shisong Ma, Mark Fredricksen, David W Galbraith, Matthew A Jenks, David Rhodes, Paul M Hasegawa, Hans J Bohnert, Robert J Joly, Ray A Bressan, Jian-Kang Zhu.   

Abstract

Salt cress (Thellungiella halophila) is a small winter annual crucifer with a short life cycle. It has a small genome (about 2 x Arabidopsis) with high sequence identity (average 92%) with Arabidopsis, and can be genetically transformed by the simple floral dip procedure. It is capable of copious seed production. Salt cress is an extremophile native to harsh environments and can reproduce after exposure to extreme salinity (500 mm NaCl) or cold to -15 degrees C. It is a typical halophyte that accumulates NaCl at controlled rates and also dramatic levels of Pro (>150 mm) during exposure to high salinity. Stomata of salt cress are distributed on the leaf surface at higher density, but are less open than the stomata of Arabidopsis and respond to salt stress by closing more tightly. Leaves of salt cress are more succulent-like, have a second layer of palisade mesophyll cells, and are frequently shed during extreme salt stress. Roots of salt cress develop both an extra endodermis and cortex cell layer compared to Arabidopsis. Salt cress, although salt and cold tolerant, is not exceptionally tolerant of soil desiccation. We have isolated several ethyl methanesulfonate mutants of salt cress that have reduced salinity tolerance, which provide evidence that salt tolerance in this halophyte can be significantly affected by individual genetic loci. Analysis of salt cress expressed sequence tags provides evidence for the presence of paralogs, missing in the Arabidopsis genome, and for genes with abiotic stress-relevant functions. Hybridizations of salt cress RNA targets to an Arabidopsis whole-genome oligonucleotide array indicate that commonly stress-associated transcripts are expressed at a noticeably higher level in unstressed salt cress plants and are induced rapidly under stress. Efficient transformation of salt cress allows for simple gene exchange between Arabidopsis and salt cress. In addition, the generation of T-DNA-tagged mutant collections of salt cress, already in progress, will open the door to a new era of forward and reverse genetic studies of extremophile plant biology.

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Year:  2004        PMID: 15247369      PMCID: PMC519085          DOI: 10.1104/pp.104.041723

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  34 in total

1.  Plant salt tolerance.

Authors:  J K Zhu
Journal:  Trends Plant Sci       Date:  2001-02       Impact factor: 18.313

Review 2.  Genetic analysis of plant salt tolerance using Arabidopsis.

Authors:  J K Zhu
Journal:  Plant Physiol       Date:  2000-11       Impact factor: 8.340

3.  Differential expression and function of Arabidopsis thaliana NHX Na+/H+ antiporters in the salt stress response.

Authors:  Shuji Yokoi; Francisco J Quintero; Beatriz Cubero; Maria T Ruiz; Ray A Bressan; Paul M Hasegawa; Jose M Pardo
Journal:  Plant J       Date:  2002-06       Impact factor: 6.417

4.  GENETIC CONTROL OF FLOWERING TIME IN ARABIDOPSIS.

Authors:  Maarten Koornneef; Carlos Alonso-Blanco; Anton J. M. Peeters; Wim Soppe
Journal:  Annu Rev Plant Physiol Plant Mol Biol       Date:  1998-06

5.  Comparative physiology of salt and water stress.

Authors:  R. Munns
Journal:  Plant Cell Environ       Date:  2002-02       Impact factor: 7.228

6.  The HIC signalling pathway links CO2 perception to stomatal development.

Authors:  J E Gray; G H Holroyd; F M van der Lee; A R Bahrami; P C Sijmons; F I Woodward; W Schuch; A M Hetherington
Journal:  Nature       Date:  2000-12-07       Impact factor: 49.962

7.  Functional activity and role of cation-efflux family members in Ni hyperaccumulation in Thlaspi goesingense.

Authors:  M W Persans; K Nieman; D E Salt
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-31       Impact factor: 11.205

8.  Activation tagging in Arabidopsis.

Authors:  D Weigel; J H Ahn; M A Blázquez; J O Borevitz; S K Christensen; C Fankhauser; C Ferrándiz; I Kardailsky; E J Malancharuvil; M M Neff; J T Nguyen; S Sato; Z Y Wang; Y Xia; R A Dixon; M J Harrison; C J Lamb; M F Yanofsky; J Chory
Journal:  Plant Physiol       Date:  2000-04       Impact factor: 8.340

9.  Global analysis of cell type-specific gene expression.

Authors:  David W Galbraith
Journal:  Comp Funct Genomics       Date:  2003

10.  Cellular organisation of the Arabidopsis thaliana root.

Authors:  L Dolan; K Janmaat; V Willemsen; P Linstead; S Poethig; K Roberts; B Scheres
Journal:  Development       Date:  1993-09       Impact factor: 6.868

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  117 in total

Review 1.  Life at the extreme: lessons from the genome.

Authors:  Dong-Ha Oh; Maheshi Dassanayake; Hans J Bohnert; John M Cheeseman
Journal:  Genome Biol       Date:  2012       Impact factor: 13.583

2.  Insights into salt tolerance from the genome of Thellungiella salsuginea.

Authors:  Hua-Jun Wu; Zhonghui Zhang; Jun-Yi Wang; Dong-Ha Oh; Maheshi Dassanayake; Binghang Liu; Quanfei Huang; Hai-Xi Sun; Ran Xia; Yaorong Wu; Yi-Nan Wang; Zhao Yang; Yang Liu; Wanke Zhang; Huawei Zhang; Jinfang Chu; Cunyu Yan; Shuang Fang; Jinsong Zhang; Yiqin Wang; Fengxia Zhang; Guodong Wang; Sang Yeol Lee; John M Cheeseman; Bicheng Yang; Bo Li; Jiumeng Min; Linfeng Yang; Jun Wang; Chengcai Chu; Shou-Yi Chen; Hans J Bohnert; Jian-Kang Zhu; Xiu-Jie Wang; Qi Xie
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-09       Impact factor: 11.205

3.  Ectopic expression of ThCYP1, a stress-responsive cyclophilin gene from Thellungiella halophila, confers salt tolerance in fission yeast and tobacco cells.

Authors:  An-Ping Chen; Gui-Ling Wang; Zhan-Liang Qu; Chun-Xia Lu; Ning Liu; Fang Wang; Gui-Xian Xia
Journal:  Plant Cell Rep       Date:  2006-09-14       Impact factor: 4.570

4.  Abiotic stress and plant genome evolution. Search for new models.

Authors:  Anna Amtmann; Hans J Bohnert; Ray A Bressan
Journal:  Plant Physiol       Date:  2005-05       Impact factor: 8.340

5.  Osmogenetics: Aristotle to Arabidopsis.

Authors:  Albino Maggio; Jian-Kang Zhu; Paul M Hasegawa; Ray A Bressan
Journal:  Plant Cell       Date:  2006-07       Impact factor: 11.277

6.  Development of an in planta method for transformation of alfalfa (Medicago sativa).

Authors:  J Troy Weeks; Jingsong Ye; Caius M Rommens
Journal:  Transgenic Res       Date:  2007-09-13       Impact factor: 2.788

7.  Tolerance to various environmental stresses conferred by the salt-responsive rice gene ONAC063 in transgenic Arabidopsis.

Authors:  Naoki Yokotani; Takanari Ichikawa; Youichi Kondou; Minami Matsui; Hirohiko Hirochika; Masaki Iwabuchi; Kenji Oda
Journal:  Planta       Date:  2009-02-19       Impact factor: 4.116

8.  Low-affinity Na+ uptake in the halophyte Suaeda maritima.

Authors:  Suo-Min Wang; Jin-Lin Zhang; Timothy J Flowers
Journal:  Plant Physiol       Date:  2007-08-31       Impact factor: 8.340

9.  The Thellungiella salsuginea tonoplast aquaporin TsTIP1;2 functions in protection against multiple abiotic stresses.

Authors:  Li-Li Wang; An-Ping Chen; Nai-Qin Zhong; Ning Liu; Xiao-Min Wu; Fang Wang; Chun-Lin Yang; Michael F Romero; Gui-Xian Xia
Journal:  Plant Cell Physiol       Date:  2013-11-09       Impact factor: 4.927

10.  ROS-mediated vascular homeostatic control of root-to-shoot soil Na delivery in Arabidopsis.

Authors:  Caifu Jiang; Eric J Belfield; Aziz Mithani; Anne Visscher; Jiannis Ragoussis; Richard Mott; J Andrew C Smith; Nicholas P Harberd
Journal:  EMBO J       Date:  2012-10-12       Impact factor: 11.598

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