2016
DOI: 10.1093/jxb/erw366
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Characterization of a novel β-barrel protein (AtOM47) from the mitochondrial outer membrane ofArabidopsis thaliana

Abstract: HighlightCharacterization of a novel β-barrel protein in Arabidopsis identifies its role in leaf senescence by mediating the transport of chloroplast breakdown products across the outer mitochondrial membrane for their recycling.

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Cited by 16 publications
(11 citation statements)
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“…Arabidopsis thaliana ecotype Columbia‐0 (Col‐0) was used as the wild‐type control for all experiments unless stated otherwise. aox1a (Giraud et al ., ); At12cys‐1 , At12cys‐2a , At12cys‐2b , ndufs4 , rug3 , tim23‐2 KO , TIM23‐2 OE (Wang et al ., ); kin10 , rao1‐2 , CDKE1‐OE (Ng et al ., ); myb29‐1 , myb29‐2 (Zhang et al ., ); mia40 (Carrie et al ., ); om47‐1 , om47‐2 (Li et al ., ); om66‐1 , OM66 OE (Zhang et al ., ); rao2‐1 , ANAC017‐OE (Ng et al ., ); rao3 (Ivanova et al ., ); WRKY15 OE , wrky33‐1 , wrky33‐2 , WRKY40 OE , wrky40‐1 , wrky42‐1 (Van Aken et al ., ); abi4‐1 (Giraud et al ., ); axr4 (Hobbie and Estelle, ); coi1‐16 (Ellis and Turner, ); eds5‐1 (Glazebrook et al ., ); ein2‐1 , etr1‐3 (Guzman and Ecker, ); gai‐1 (Koorneef et al ., ); gai‐t6/rga‐t2/rgl1‐1/rgl2‐1/rgl3‐1 (Feng et al ., ); yucca (Zhao et al ., ). The coding sequence of At12CYS‐1 (At5 g64400) and At12CYS‐2 (At5 g09570) was cloned to pk7WG2 using the Gateway methods to obtain the At12CYS‐1‐OE and At12CYS‐2‐OE overexpression constructs, respectively.…”
Section: Methodsmentioning
confidence: 99%
“…Arabidopsis thaliana ecotype Columbia‐0 (Col‐0) was used as the wild‐type control for all experiments unless stated otherwise. aox1a (Giraud et al ., ); At12cys‐1 , At12cys‐2a , At12cys‐2b , ndufs4 , rug3 , tim23‐2 KO , TIM23‐2 OE (Wang et al ., ); kin10 , rao1‐2 , CDKE1‐OE (Ng et al ., ); myb29‐1 , myb29‐2 (Zhang et al ., ); mia40 (Carrie et al ., ); om47‐1 , om47‐2 (Li et al ., ); om66‐1 , OM66 OE (Zhang et al ., ); rao2‐1 , ANAC017‐OE (Ng et al ., ); rao3 (Ivanova et al ., ); WRKY15 OE , wrky33‐1 , wrky33‐2 , WRKY40 OE , wrky40‐1 , wrky42‐1 (Van Aken et al ., ); abi4‐1 (Giraud et al ., ); axr4 (Hobbie and Estelle, ); coi1‐16 (Ellis and Turner, ); eds5‐1 (Glazebrook et al ., ); ein2‐1 , etr1‐3 (Guzman and Ecker, ); gai‐1 (Koorneef et al ., ); gai‐t6/rga‐t2/rgl1‐1/rgl2‐1/rgl3‐1 (Feng et al ., ); yucca (Zhao et al ., ). The coding sequence of At12CYS‐1 (At5 g64400) and At12CYS‐2 (At5 g09570) was cloned to pk7WG2 using the Gateway methods to obtain the At12CYS‐1‐OE and At12CYS‐2‐OE overexpression constructs, respectively.…”
Section: Methodsmentioning
confidence: 99%
“…Notably, the dgs1-2 null mutant did not affect the abundance of any protein or the activity of the respiratory chain ( Figures 5A and 5B). However, both the dgs1-1 mutant and the dgs1-1 Comp (L) line with protein levels comparable to the wild type showed decreased abundance of an outer membrane (OM) b-barrel protein in plant mitochondria (OM47; Li et al, 2016b), TIM44, and AOX ( Figure 5A). The consistent decrease in abundance of TOM20s ( Figure 2B), OM47, TIM44, and AOX ( Figure 5A) in all lines expressing the dgs1-1 mutant protein indicates that the mutated dgs1-1 protein has an effect on specific proteins or pathways.…”
Section: The Dgs1-1 Mutation Alters Mitochondrial Lipid Compositionmentioning
confidence: 99%
“…The total chlorophyll content was measured as described previously (Li et al, 2016b). The chlorophyll fluorescence F v /F m (maximum quantum yield of PSII) was pulsed with 120 mmol m 22 s 21 of actinic light using the IMAGING-PAM M-series Chlorophyll Fluorescence System (Walz) after a 20 min of dark acclimation as described previously (Rossel et al, 2006).…”
Section: Chlorophyll Analysis and Fluorescencementioning
confidence: 99%
“…AsA and DHA levels were determined as previously described [7]. A dark-induced senescence assay was performed where two-week-old Arabidopsis seedlings were subjected to continuous dark treatment for 3 d and 6 d and then light recovery for 16 h. Chlorophyll content determination in Arabidopsis seedlings were conducted as described elsewhere [31,72]. The expression levels of flowering-related genes such as GI, FVE, LFY, CO, FT, AP1, SOC1, and FLC; and SAGs, including PIFs (PIF3, PIF4, and PIF5), SENs (SEN1 and SEN4), SAG20, TFs (WRKY6, NAP, and NAC2), cell-programmed death genes (ACD1 and PDCD5), and PHENOPHYTIN PHEOPHORBIDE HYDROLASE (PPH), were determined by qRT-PCR using Arabidopsis thaliana 18S ribosomal RNA (At18SrRNA) and Arabidopsis thaliana Actin 2 (AtACTIN2) genes as reference genes to normalize the qRT-PCR data, with the gene-specific primers listed in Supplementary Table S4.…”
Section: Functional Analysis Of Ghao1a In Arabidopsismentioning
confidence: 99%