1998
DOI: 10.1101/gad.12.19.3059
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Pleiotropic control of glucose and hormone responses by PRL1, a nuclear WD protein, in Arabidopsis

Abstract: The prl1 mutation localized by T-DNA tagging on Arabidopsis chromosome 4-44 confers hypersensitivity to glucose and sucrose. The prl1 mutation results in transcriptional derepression of glucose responsive genes defining a novel suppressor function in glucose signaling. The prl1 mutation also augments the sensitivity of plants to growth hormones including cytokinin, ethylene, abscisic acid, and auxin; stimulates the accumulation of sugars and starch in leaves; and inhibits root elongation. PRL1 encodes a regula… Show more

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Cited by 238 publications
(273 citation statements)
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“…Although subsequent studies did not confirm in vivo formation of a CRK5-PRL1 complex under normal growth conditions, we found that inactivation of the CRK5 gene by a T-DNA insertion in the MPIZ mutant line 38225 (crk5-1; Ríos et al, 2002; see Supplemental Figure 1A online) resulted in reduced primary root elongation ( Figure 1A), analogously to the prl1 mutation (Németh et al, 1998). By contrast, a second T-DNA insertion in the CRK5 gene (Salk_003774, crk5-2) obtained from the SIGnAL collection (Alonso et al, 2003) failed to confer a root elongation detect.…”
Section: Inactivation Of Crk5 Results In Delayed Gravitropic Responsesmentioning
confidence: 84%
See 1 more Smart Citation
“…Although subsequent studies did not confirm in vivo formation of a CRK5-PRL1 complex under normal growth conditions, we found that inactivation of the CRK5 gene by a T-DNA insertion in the MPIZ mutant line 38225 (crk5-1; Ríos et al, 2002; see Supplemental Figure 1A online) resulted in reduced primary root elongation ( Figure 1A), analogously to the prl1 mutation (Németh et al, 1998). By contrast, a second T-DNA insertion in the CRK5 gene (Salk_003774, crk5-2) obtained from the SIGnAL collection (Alonso et al, 2003) failed to confer a root elongation detect.…”
Section: Inactivation Of Crk5 Results In Delayed Gravitropic Responsesmentioning
confidence: 84%
“…CRK5 (called alternatively PIP-D) was originally identified in yeast two-hybrid and in vitro protein binding assays as a potential interaction partner of the C-terminal WD40-repeat domain of nuclear PRL1 protein, a subunit of the spliceosome-activating complex (Németh et al, 1998;Koncz et al, 2012). Although subsequent studies did not confirm in vivo formation of a CRK5-PRL1 complex under normal growth conditions, we found that inactivation of the CRK5 gene by a T-DNA insertion in the MPIZ mutant line 38225 (crk5-1; Ríos et al, 2002; see Supplemental Figure 1A online) resulted in reduced primary root elongation ( Figure 1A), analogously to the prl1 mutation (Németh et al, 1998).…”
Section: Inactivation Of Crk5 Results In Delayed Gravitropic Responsesmentioning
confidence: 99%
“…The PRL1 gene codes for a WD-protein that, by analogy to COP1, functions as a negative regulator of a set of light-, hormone-, and stress-regulated genes (Ne¨meth et al 1998). Mutation of PLR1 results in complex phenotypic defects, including the inhibition of hypocotyl elongation in the dark.…”
Section: The Cpd Gene Is Regulated By Prl1 In Arabidopsismentioning
confidence: 99%
“…Genetic screening for PRL1 interacting proteins in the yeast two-hybrid system revealed that PRL1 speci¢cally binds a novel a-importin, ATHKAP2 (Ne¨meth et al 1998). ATHKAP2 does not bind to proteins containing monopartite and bipartite nuclear localization signals (NLS).…”
Section: Prl1 Is a Conserved A-importin-binding Nuclear Protein Thatmentioning
confidence: 99%
“…Transformation of plasmids into yeast was done according to the LiAc transformation method [19]. STK01 and STK03 constructs were cloned into the bait vector pAS2.1 (Clontech), and yeast-2-hybrid screening of an Arabidopsis cell suspension culture cDNA library in pACT2.1 [20] was carried out according to [21].…”
Section: Yeast Two-hybrid Screeningmentioning
confidence: 99%