scholarly journals Cross-species functional diversity within the PIN auxin efflux protein family

2016 ◽  
Author(s):  
Devin Lee O’Connor ◽  
Samuel Elton ◽  
Fabrizio Ticchiarelli ◽  
Mon Mandy Hsia ◽  
John Vogel ◽  
...  

AbstractIn Arabidopsis, development during flowering is coordinated by transport of the hormone auxin mediated by polar-localized PIN-FORMED1 (AtPIN1). However Arabidopsis has lost a PIN clade sister to AtPIN1, Sister-of-PIN1 (SoPIN1), which is conserved in flowering plants. We previously proposed that the AtPIN1 organ initiation and vein patterning functions are split between the SoPIN1 and PIN1 clades in grasses. Here we show that in the grass Brachypodium sopin1 mutants have organ initiation defects similar to Arabidopsis atpin1, while loss of PIN1 function in Brachypodium has little effect on organ initiation but alters stem growth. Heterologous expression of Brachypodium SoPIN1 and PIN1b in Arabidopsis provides further evidence of functional specificity. SoPIN1 but not PIN1b can mediate flower formation in null atpin1 mutants, although both can complement a missense allele. The behavior of SoPIN1 and PIN1b in Arabidopsis illustrates how membrane and tissue-level accumulation, transport activity, and interaction contribute to PIN functional specificity.

eLife ◽  
2017 ◽  
Vol 6 ◽  
Author(s):  
Devin Lee O'Connor ◽  
Samuel Elton ◽  
Fabrizio Ticchiarelli ◽  
Mon Mandy Hsia ◽  
John P Vogel ◽  
...  

In Arabidopsis, development during flowering is coordinated by transport of the hormone auxin mediated by polar-localized PIN-FORMED1 (AtPIN1). However Arabidopsis has lost a PIN clade sister to AtPIN1, Sister-of-PIN1 (SoPIN1), which is conserved in flowering plants. We previously proposed that the AtPIN1 organ initiation and vein patterning functions are split between the SoPIN1 and PIN1 clades in grasses. Here we show that in the grass Brachypodium sopin1 mutants have organ initiation defects similar to Arabidopsis atpin1, while loss of PIN1 function in Brachypodium has little effect on organ initiation but alters stem growth. Heterologous expression of Brachypodium SoPIN1 and PIN1b in Arabidopsis provides further evidence of functional specificity. SoPIN1 but not PIN1b can mediate flower formation in null atpin1 mutants, although both can complement a missense allele. The behavior of SoPIN1 and PIN1b in Arabidopsis illustrates how membrane and tissue-level accumulation, transport activity, and interaction contribute to PIN functional specificity.


1982 ◽  
Vol 30 (3) ◽  
pp. 173-177
Author(s):  
J.A. Schipper

Bulbs of the iris cvs Ideal (8-9 or 10 cm circumference) and Prof. Blaauw (9-10 or 11 cm circumference) for early forcing were exposed to smoke from burning damp wheat straw during the first or second week of storage at 35 deg C after lifting. Smoke treatment was applied for 1, 3 or 5 days; gas analyses for ethylene, CO and O2 showed considerable variations in composition. With Ideal, treatment reduced the % non-flowering plants (in terms of bud blast for the 10-cm bulbs and three-leaved plants for the 8-9 cm bulbs) compared with controls; the larger bulbs also flowered earlier than those of controls. Fewer leaves than normal were produced. Flowering % in Prof. Blaauw was improved slightly by treatment, but earliness was not increased. No difference in effect was observed between the 2 treatment dates or the 3 durations. [For earlier work see HcA 51, 480.] (Abstract retrieved from CAB Abstracts by CABI’s permission)


1973 ◽  
Vol 21 (4) ◽  
pp. 245-255
Author(s):  
S.J. Wellensiek

Several selected S. armeria lines differing in their reaction to GA3 were treated with GA3 at various concentrations under short-day (SD) or long-day conditions. With SD treatment one application of GA3 at high concentration (10 000 p.p.m. or greater) induced flower formation in certain lines. Stem elongation increased with GA3 concentration and with plant age and was much greater on flowering plants than on non-flowering ones. [For previous related work see HcA 41, 4400.]. (Abstract retrieved from CAB Abstracts by CABI’s permission)


2019 ◽  
Author(s):  
Sarah Zinecker ◽  
Mario Jakob ◽  
Ralf Bernd Klösgen

AbstractWe have established an experimental system for the functional analysis of thylakoidal TatB, a component of the membrane-integral TatBC receptor complex of the thylakoidal Twin-arginine protein transport (Tat1) machinery. For this purpose, the intrinsic TatB activity of isolated pea thylakoids was inhibited by affinity-purified antibodies and substituted by supplementing the assays with TatB protein either obtained by in vitro translation or purified after heterologous expression in E. coli. Tat transport activity of such reconstituted thylakoids, which was analyzed with the authentic Tat substrate pOEC16, reached routinely 20 - 25% of the activity of mock-treated thylakoid vesicles analysed in parallel. In contrast, supplementation of the assays with the purified antigen comprising all but the N-terminal transmembrane helix of thylakoidal TatB did not result in Tat transport reconstitution which confirms that transport relies strictly on the activity of the TatB protein added and is not due to restoration of the intrinsic TatB activity by antibody release. Unexpectedly, even a mutant TatB protein (TatB,E10C) assumed to be incapable of assembling into the TatBC receptor complex showed low but considerable transport reconstitution underlining the sensitivity of the approach and its suitability for further functional mutant analyses. Finally, quantification of TatB demand suggests that TatA and TatB are required in approximately equimolar amounts to achieve Tat-dependent thylakoid transport.


Planta ◽  
1979 ◽  
Vol 145 (2) ◽  
pp. 175-180 ◽  
Author(s):  
Jeffrey C. Suttle ◽  
Jan A. D. Zeevaart

2020 ◽  
Author(s):  
Paula J. Rudall
Keyword(s):  

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