Literature DB >> 11812174

Developmental genetics and evolution of symbiotic structures in nitrogen-fixing nodules and arbuscular mycorrhiza.

Nikolai A Provorov1, Alex Yu Borisov, Igor A Tikhonovich.   

Abstract

Genetic and molecular mechanisms of development are compared for two major plant-microbe endosymbioses: N(2)-fixing nodules (with rhizobia or actinomycetes Frankia) and arbuscular mycorrhiza (with Glomales fungi). Development from the primordia formed de novo in root tissues is common for all known types of N(2)-fixing nodules. However, their structure varies greatly with respect to: (i) tissue topology (location of vascular bundles is peripherical in legumes or central in non-legumes); (ii) position of nodule primordium (inner or outer cortex in legumes, pericycle in non-legumes); (iii) stability of apical meristem (persistent in the indeterminate nodules, transient in the determinate ones). In addition, legumes vary in ability to form compartments harboring endosymbiotic rhizobia and located intercellularly (infection threads) and intracellularly (symbiosomes). Using pea (Pisum sativum) symbiotic mutants, the nodule developmental program is dissected into a range of spatially and temporarily differentiated steps comprising four sub-programs (development of endosymbiotic compartments; nodule histogenesis; autoregulation of nodulation; bacteroid differentiation). The developmental mutations are suggested in some cases to reverse the endosymbiotic system into the morphologically simpler forms some of which may correspond to the ancestral stages of nodule evolution. The origin of legume-rhizobial and actinorhizal symbioses is suggested to be based on a set of preadaptations many of which had been evolved in angiosperms during coevolution with arbuscular mycorrhizal fungi (e.g., inter- and intracellular maintenance of symbionts, their control via defence-like reactions and recognition of chitin-like molecules). An analysis of parallel morphological variation in symbiotic mutants and wild-growing legume species enables us to reconstruct the major stages of evolution for N(2)-fixing symbioses. Copyright 2002 Academic Press.

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Year:  2002        PMID: 11812174     DOI: 10.1006/jtbi.2001.2453

Source DB:  PubMed          Journal:  J Theor Biol        ISSN: 0022-5193            Impact factor:   2.691


  10 in total

1.  Nonlegumes, legumes, and root nodules harbor different arbuscular mycorrhizal fungal communities.

Authors:  Tanja R Scheublin; Karyn P Ridgway; J Peter W Young; Marcel G A van der Heijden
Journal:  Appl Environ Microbiol       Date:  2004-10       Impact factor: 4.792

2.  Overlaps in the transcriptional profiles of Medicago truncatula roots inoculated with two different Glomus fungi provide insights into the genetic program activated during arbuscular mycorrhiza.

Authors:  Natalija Hohnjec; Martin F Vieweg; Alfred Pühler; Anke Becker; Helge Küster
Journal:  Plant Physiol       Date:  2005-03-18       Impact factor: 8.340

3.  Characterization of the Lotus japonicus symbiotic mutant lot1 that shows a reduced nodule number and distorted trichomes.

Authors:  Yasuhiro Ooki; Mari Banba; Koji Yano; Jumpei Maruya; Shusei Sato; Satoshi Tabata; Kazuhiko Saeki; Makoto Hayashi; Masayoshi Kawaguchi; Katsura Izui; Shingo Hata
Journal:  Plant Physiol       Date:  2005-03-25       Impact factor: 8.340

4.  Effects of co-inoculation with arbuscular mycorrhizal fungi and rhizobia on fungal occupancy in chickpea root and nodule determined by real-time PCR.

Authors:  Alireza Tavasolee; Naser Aliasgharzad; Gholam Reza Salehi; Mohsen Mardi; Ahmad Asgharzadeh; Sepide Akbarivala
Journal:  Curr Microbiol       Date:  2011-05-22       Impact factor: 2.188

5.  Transcriptome analysis of soybean (Glycine max) root genes differentially expressed in rhizobial, arbuscular mycorrhizal, and dual symbiosis.

Authors:  Kazunori Sakamoto; Natsuko Ogiwara; Tomomitsu Kaji; Yurie Sugimoto; Mitsuru Ueno; Masatoshi Sonoda; Akihiro Matsui; Junko Ishida; Maho Tanaka; Yasushi Totoki; Kazuo Shinozaki; Motoaki Seki
Journal:  J Plant Res       Date:  2019-06-05       Impact factor: 2.629

6.  Effect of microbial inoculants on the indigenous actinobacterial endophyte population in the roots of wheat as determined by terminal restriction fragment length polymorphism.

Authors:  Vanessa M Conn; Christopher M M Franco
Journal:  Appl Environ Microbiol       Date:  2004-11       Impact factor: 4.792

7.  Two genes encoding different truncated hemoglobins are regulated during root nodule and arbuscular mycorrhiza symbioses of Medicago truncatula.

Authors:  Martin F Vieweg; Natalija Hohnjec; Helge Küster
Journal:  Planta       Date:  2004-10-23       Impact factor: 4.116

8.  Analysis of the endophytic actinobacterial population in the roots of wheat (Triticum aestivum L.) by terminal restriction fragment length polymorphism and sequencing of 16S rRNA clones.

Authors:  Vanessa M Conn; Christopher M M Franco
Journal:  Appl Environ Microbiol       Date:  2004-03       Impact factor: 4.792

9.  Strategy diversity stabilizes mutualism through investment cycles, phase polymorphism, and spatial bubbles.

Authors:  Gergely Boza; Adám Kun; István Scheuring; Ulf Dieckmann
Journal:  PLoS Comput Biol       Date:  2012-11-15       Impact factor: 4.475

10.  The mycorrhiza-dependent defensin MtDefMd1 of Medicago truncatula acts during the late restructuring stages of arbuscule-containing cells.

Authors:  Marian Uhe; Claudia Hogekamp; Rico M Hartmann; Natalija Hohnjec; Helge Küster
Journal:  PLoS One       Date:  2018-01-25       Impact factor: 3.240

  10 in total

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