Regulation of Nodule Development by Short- and Long-Distance Auxin Transport Control

2015 ◽  
pp. 465-474 ◽  
Author(s):  
Ulrike Mathesius ◽  
Jian Jin ◽  
Giel E. Noorden ◽  
Liang P. J. Ng ◽  
Anton P. Wasson
Plants ◽  
2020 ◽  
Vol 9 (8) ◽  
pp. 940 ◽  
Author(s):  
Jesse J. Küpers ◽  
Lisa Oskam ◽  
Ronald Pierik

Light absorption by plants changes the composition of light inside vegetation. Blue (B) and red (R) light are used for photosynthesis whereas far-red (FR) and green light are reflected. A combination of UV-B, blue and R:FR-responsive photoreceptors collectively measures the light and temperature environment and adjusts plant development accordingly. This developmental plasticity to photoreceptor signals is largely regulated through the phytohormone auxin. The phytochrome, cryptochrome and UV Resistance Locus 8 (UVR8) photoreceptors are inactivated in shade and/or elevated temperature, which releases their repression of Phytochrome Interacting Factor (PIF) transcription factors. Active PIFs stimulate auxin synthesis and reinforce auxin signalling responses through direct interaction with Auxin Response Factors (ARFs). It was recently discovered that shade-induced hypocotyl elongation and petiole hyponasty depend on long-distance auxin transport towards target cells from the cotyledon and leaf tip, respectively. Other responses, such as phototropic bending, are regulated by auxin transport and signalling across only a few cell layers. In addition, photoreceptors can directly interact with components in the auxin signalling pathway, such as Auxin/Indole Acetic Acids (AUX/IAAs) and ARFs. Here we will discuss the complex interactions between photoreceptor and auxin signalling, addressing both mechanisms and consequences of these highly interconnected pathways.


2006 ◽  
Vol 140 (4) ◽  
pp. 1494-1506 ◽  
Author(s):  
Giel E. van Noorden ◽  
John J. Ross ◽  
James B. Reid ◽  
Barry G. Rolfe ◽  
Ulrike Mathesius

2004 ◽  
Vol 17 (12) ◽  
pp. 1283-1293 ◽  
Author(s):  
Emmanouil Flemetakis ◽  
Rodica C. Efrose ◽  
Guilhem Desbrosses ◽  
Maria Dimou ◽  
Costas Delis ◽  
...  

Putrescine and other polyamines are produced by two alternative pathways in plants. One pathway starts with the enzyme arginine decarboxylase (ADC; EC 4.1.1.19), the other with ornithine decarboxylase (ODC; EC 4.1.1.17). Metabolite profiling of nitrogen-fixing Lotus japonicus nodules, using gas chromatography coupled to mass spectrometry, revealed a two- to sixfold increase in putrescine levels in mature nodules compared with other organs. Genes involved in polyamine biosynthesis in L. japonicus nodules were identified by isolating cDNA clones encoding ADC (LjADC1) and ODC (LjODC) from a nodule library. Searches of the public expressed sequence tag databases revealed the presence of a second gene encoding ADC (LjADC2). Real-time reverse-transcription-polymerase chain reaction analysis showed that LjADC1 and LjADC2 were expressed throughout the plant, while LjODC transcripts were detected only in nodules and roots. Induction of LjODC and LjADC gene expression during nodule development preceded symbiotic nitrogen fixation. Transcripts accumulation was maximal at 10 days postinfection, when a 6.5-fold increase in the transcript levels of LjODC was observed in comparison with the uninfected roots, while a twofold increase in the transcript levels of LjADC1 and LjADC2 was detected. At later stages of nodule development, transcripts for ADC drastically declined, while in the case of ODC, transcript accumulation was higher than that in roots until after 21 days postinfection. The expression profile of genes involved in putrescine biosynthesis correlated well with the expression patterns of genes involved in cell division and expansion, including a L. japonicus Cyclin D3 and an α-expansin gene. Spatial localization of LjODC and LjADC1 gene transcripts in developing nodules revealed that both transcripts were expressed in nodule inner cortical cells and in the central tissue. High levels of LjADC1 transcripts were also observed in both nodule and connecting root vascular tissue, suggesting that putrescine and other polyamines may be subject to long-distance transport. Our results indicate that polyamines are primarily involved in physiological and cellular processes involved in nodule development, rather than in processes that support directly symbiotic nitrogen fixation and assimilation.


1983 ◽  
Vol 61 (6) ◽  
pp. 1768-1774 ◽  
Author(s):  
Suzanne Lachaud

The application, in the middle of April, of a mixture of IAA (10−4 M) and GA3 (10−4 M), to apical stem of young beeches, disbudded more than 1 month ago, brings about the formation of an unusual early wood, composed of small xylary elements only, on a short distance. If the phytohormones are applied immediately on the following day after disbudding, the young trees produce normal early wood, on a long distance. GA3 applied alone has hardly any effect on cambial reactivation; IAA applied alone stimulates less cambial reactivation and xylogenesis than the mixture of IAA and GA3. The study of [3H]-IAA transport in apical shoots of the same trees shows that beeches disbudded 1 month ago have lost the ability to activate the auxin transport. Disbudding, carried out in the middle or at the end of the preactivation phase, affects the IAA transport system within a few days; a further exogenous phytohormone application cannot then replace buds and promote the renewal of cambial activity. In young beeches, the resumption of tissue ability to polarize the auxin transport, which in February characterizes the beginning of the preactivation phase, depends on buds; the maintenance and development of this ability are related to their presence.


eLife ◽  
2014 ◽  
Vol 3 ◽  
Author(s):  
Melina Zourelidou ◽  
Birgit Absmanner ◽  
Benjamin Weller ◽  
Inês CR Barbosa ◽  
Björn C Willige ◽  
...  

The development and morphology of vascular plants is critically determined by synthesis and proper distribution of the phytohormone auxin. The directed cell-to-cell distribution of auxin is achieved through a system of auxin influx and efflux transporters. PIN-FORMED (PIN) proteins are proposed auxin efflux transporters, and auxin fluxes can seemingly be predicted based on the—in many cells—asymmetric plasma membrane distribution of PINs. Here, we show in a heterologous Xenopus oocyte system as well as in Arabidopsis thaliana inflorescence stems that PIN-mediated auxin transport is directly activated by D6 PROTEIN KINASE (D6PK) and PINOID (PID)/WAG kinases of the Arabidopsis AGCVIII kinase family. At the same time, we reveal that D6PKs and PID have differential phosphosite preferences. Our study suggests that PIN activation by protein kinases is a crucial component of auxin transport control that must be taken into account to understand auxin distribution within the plant.


2007 ◽  
Vol 85 (12) ◽  
pp. 1147-1157 ◽  
Author(s):  
Mathias Schuetz ◽  
Afsaneh Haghighi-Kia ◽  
Carol L. Wenzel ◽  
Jim Mattsson

Vascular tissues are of particular importance to terrestrial plants as they allow long-distance transport within the plant and also provide support for upright growth. Nowhere are these traits more obvious than in tree species. Here we have evaluated the role of auxin transport in the differentiation of primary and secondary vascular tissues in a tree species, trembling aspen ( Populus tremuloides Michx). We found that a partial inhibition of auxin transport resulted in increased width and numbers of veins in leaves. A similar vascular overgrowth was observed during early secondary vascular differentiation of stems. This stem overgrowth consisted almost entirely of early differentiation of metaxylem and fibers. We hypothesize that the early differentiation of metaxylem and fibers results from inhibitor-induced accumulation of auxin in stems and that the differentiation of these tissues requires higher levels of auxin exposure than protoxylem. The controlled conditions used in this study also provide a framework for reverse genetics approaches to identify genes involved in vascular differentiation based on elevated expression in tissues developing vascular overgrowth.


2012 ◽  
Vol 194 (3) ◽  
pp. 704-715 ◽  
Author(s):  
Michael Renton ◽  
Jim Hanan ◽  
Brett J. Ferguson ◽  
Christine A. Beveridge

2019 ◽  
Vol 71 (4) ◽  
pp. 1562-1573 ◽  
Author(s):  
Jason L P Ng ◽  
Astrid Welvaert ◽  
Jiangqi Wen ◽  
Rujin Chen ◽  
Ulrike Mathesius

Abstract The development of root nodules leads to an increased auxin response in early nodule primordia, which is mediated by changes in acropetal auxin transport in some legumes. Here, we investigated the role of root basipetal auxin transport during nodulation. Rhizobia inoculation significantly increased basipetal auxin transport in both Medicago truncatula and Lotus japonicus. In M. truncatula, this increase was dependent on functional Nod factor signalling through NFP, NIN, and NSP2, as well as ethylene signalling through SKL. To test whether increased basipetal auxin transport is required for nodulation, we examined a loss-of-function mutant of the M. truncatula PIN2 gene. The Mtpin2 mutant exhibited a reduction in basipetal auxin transport and an agravitropic phenotype. Inoculation of Mtpin2 roots with rhizobia still led to a moderate increase in basipetal auxin transport, but the mutant nodulated normally. No clear differences in auxin response were observed during nodule development. Interestingly, inoculation of wild-type roots increased lateral root numbers, whereas inoculation of Mtpin2 mutants resulted in reduced lateral root numbers compared with uninoculated roots. We conclude that the MtPIN2 auxin transporter is involved in basipetal auxin transport, that its function is not essential for nodulation, but that it plays an important role in the control of lateral root development.


Sign in / Sign up

Export Citation Format

Share Document