In site bioimaging of hydrogen sulfide uncovers its pivotal role in regulating nitric oxide-induced lateral root formation.
Hydrogen sulfide (H2S) is an important gasotransmitter in mammals. Despite physiological changes induced by exogenous H2S donor NaHS to plants, whether and how H2S works as a true cellular signal in plants need to be examined. A self-developed specific fluorescent probe (WSP-1) was applied to track...
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2014-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC3937356?pdf=render |
id |
doaj-2d21de13e4ad4b988748a77e8311fc86 |
---|---|
record_format |
Article |
spelling |
doaj-2d21de13e4ad4b988748a77e8311fc862020-11-25T01:24:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0192e9034010.1371/journal.pone.0090340In site bioimaging of hydrogen sulfide uncovers its pivotal role in regulating nitric oxide-induced lateral root formation.Yan-Jun LiJian ChenMing XianLi-Gang ZhouFengxiang X HanLi-Jun GanZhi-Qi ShiHydrogen sulfide (H2S) is an important gasotransmitter in mammals. Despite physiological changes induced by exogenous H2S donor NaHS to plants, whether and how H2S works as a true cellular signal in plants need to be examined. A self-developed specific fluorescent probe (WSP-1) was applied to track endogenous H2S in tomato (Solanum lycopersicum) roots in site. Bioimaging combined with pharmacological and biochemical approaches were used to investigate the cross-talk among H2S, nitric oxide (NO), and Ca(2+) in regulating lateral root formation. Endogenous H2S accumulation was clearly associated with primordium initiation and lateral root emergence. NO donor SNP stimulated the generation of endogenous H2S and the expression of the gene coding for the enzyme responsible for endogenous H2S synthesis. Scavenging H2S or inhibiting H2S synthesis partially blocked SNP-induced lateral root formation and the expression of lateral root-related genes. The stimulatory effect of SNP on Ca(2+) accumulation and CaM1 (calmodulin 1) expression could be abolished by inhibiting H2S synthesis. Ca(2+) chelator or Ca(2+) channel blocker attenuated NaHS-induced lateral root formation. Our study confirmed the role of H2S as a cellular signal in plants being a mediator between NO and Ca(2+) in regulating lateral root formation.http://europepmc.org/articles/PMC3937356?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yan-Jun Li Jian Chen Ming Xian Li-Gang Zhou Fengxiang X Han Li-Jun Gan Zhi-Qi Shi |
spellingShingle |
Yan-Jun Li Jian Chen Ming Xian Li-Gang Zhou Fengxiang X Han Li-Jun Gan Zhi-Qi Shi In site bioimaging of hydrogen sulfide uncovers its pivotal role in regulating nitric oxide-induced lateral root formation. PLoS ONE |
author_facet |
Yan-Jun Li Jian Chen Ming Xian Li-Gang Zhou Fengxiang X Han Li-Jun Gan Zhi-Qi Shi |
author_sort |
Yan-Jun Li |
title |
In site bioimaging of hydrogen sulfide uncovers its pivotal role in regulating nitric oxide-induced lateral root formation. |
title_short |
In site bioimaging of hydrogen sulfide uncovers its pivotal role in regulating nitric oxide-induced lateral root formation. |
title_full |
In site bioimaging of hydrogen sulfide uncovers its pivotal role in regulating nitric oxide-induced lateral root formation. |
title_fullStr |
In site bioimaging of hydrogen sulfide uncovers its pivotal role in regulating nitric oxide-induced lateral root formation. |
title_full_unstemmed |
In site bioimaging of hydrogen sulfide uncovers its pivotal role in regulating nitric oxide-induced lateral root formation. |
title_sort |
in site bioimaging of hydrogen sulfide uncovers its pivotal role in regulating nitric oxide-induced lateral root formation. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2014-01-01 |
description |
Hydrogen sulfide (H2S) is an important gasotransmitter in mammals. Despite physiological changes induced by exogenous H2S donor NaHS to plants, whether and how H2S works as a true cellular signal in plants need to be examined. A self-developed specific fluorescent probe (WSP-1) was applied to track endogenous H2S in tomato (Solanum lycopersicum) roots in site. Bioimaging combined with pharmacological and biochemical approaches were used to investigate the cross-talk among H2S, nitric oxide (NO), and Ca(2+) in regulating lateral root formation. Endogenous H2S accumulation was clearly associated with primordium initiation and lateral root emergence. NO donor SNP stimulated the generation of endogenous H2S and the expression of the gene coding for the enzyme responsible for endogenous H2S synthesis. Scavenging H2S or inhibiting H2S synthesis partially blocked SNP-induced lateral root formation and the expression of lateral root-related genes. The stimulatory effect of SNP on Ca(2+) accumulation and CaM1 (calmodulin 1) expression could be abolished by inhibiting H2S synthesis. Ca(2+) chelator or Ca(2+) channel blocker attenuated NaHS-induced lateral root formation. Our study confirmed the role of H2S as a cellular signal in plants being a mediator between NO and Ca(2+) in regulating lateral root formation. |
url |
http://europepmc.org/articles/PMC3937356?pdf=render |
work_keys_str_mv |
AT yanjunli insitebioimagingofhydrogensulfideuncoversitspivotalroleinregulatingnitricoxideinducedlateralrootformation AT jianchen insitebioimagingofhydrogensulfideuncoversitspivotalroleinregulatingnitricoxideinducedlateralrootformation AT mingxian insitebioimagingofhydrogensulfideuncoversitspivotalroleinregulatingnitricoxideinducedlateralrootformation AT ligangzhou insitebioimagingofhydrogensulfideuncoversitspivotalroleinregulatingnitricoxideinducedlateralrootformation AT fengxiangxhan insitebioimagingofhydrogensulfideuncoversitspivotalroleinregulatingnitricoxideinducedlateralrootformation AT lijungan insitebioimagingofhydrogensulfideuncoversitspivotalroleinregulatingnitricoxideinducedlateralrootformation AT zhiqishi insitebioimagingofhydrogensulfideuncoversitspivotalroleinregulatingnitricoxideinducedlateralrootformation |
_version_ |
1725117818415874048 |