Molecular-Genetic Analysis of Osmoregulation, Osmotic Adjustment and Growth in Arabidopsis

Bray, Elizabeth

The University of Chicago, Chicago Illinois

关键词: Abscisic Acid;    Chromatin;    Chromosomes;    Exons;    Solutes;   

DOI  :  10.2172/951904
RP-ID  :  None
RP-ID  :  FG02-04ER15615
RP-ID  :  951904

美国|英语

来源: UNT Digital Library

【 摘 要 】

The molecular mechanism by which plants control cellular solute and water content, called osmoregulation, is critical for cell expansion and survival, particularly in response to cellular water deficit or low water potential. Two loci, lwr1 and lwr2 (low water potential response), that affect osmoregulation were isolated as part of a larger screen to identify mutants with alterations in low water potential-induced proline accumulation. When seedlings of lwr2 were exposed to a steady low water potential stress over a period of several days using PEG-infused agar plates, the mutants had lesser proline accumulation and osmotic adjustment than the wild type, Ben. A mapping population was raised but it was not possible to reliably identify the mutants in the population and thus could not be used for mapping. The mutant lwr1 was mapped and the gene identified. The mutant lwr1 had greater accumulation of proline, higher total solute content, greater osmotic adjustment at low water potential, altered abscisic acid content, and increased sensitivity to applied abscisic acid with respect to Pro content than the wild type, Ben, when the water potential was decreased over a period of several days using PEG-infused agar plates. lwr1 also had altered growth and morphology, including defects in trichome branching with the majority of the trichomes having a single point, shortened siliques which were crooked, and significantly lengthened time to flowering. Using bulk segregant analysis, the lwr1 loci was mapped to the lower arm of chromosome II, near the marker nga168. Further detailed fine mapping located the mutation to the gene PKL, At2g25170, which was previously identified as a gene involved in altered root development. PKL encodes a chromatin remodeling factor. The mutation in lwr1 introduced a stop codon in the 14th exon of At2g25170. The mutant was not complemented by 4 other known mutants having a disrupted PKL gene confirming the placement of this mutation in lwr1. In response to ABA treatment, lwr1 and 5 different mutants in At2g25170, in two different genetic backgrounds, had elevated proline content compared to the wild type. Proline levels of lwr1 in response to water-deficit were not the same as in the originally published mutant; lwr1 and other mutants in At2g25170 had lower proline content than wild type in response to water deficit. A series of microarray hybridizations have been completed comparing control and PEG-induced stress in lwr1, lwr2 and the wild type. Analyses of these data are ongoing and are expected to shed light on the gene mutated in lwr2 and to indicate the extent of changed of gene expression that are involved in the response of lwr1 to water deficit stress. In addition, microarray experiments were completed on ABA treatments and ABA and stress treatments combined for lwr1 in order to further explore the role of ABA in plant water-deficit stress.