4.8 Article

Arabidopsis ribosomal proteins control vacuole trafficking and developmental programs through the regulation of lipid metabolism

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1422656112

关键词

ribosomal mutants; lipid metabolism; vacuole trafficking; auxin response

资金

  1. National Science Foundation [EPS 0236913, MCB 0455318, DBI 0521587]
  2. Kansas Technology Enterprise Corporation
  3. K-IDeA Networks of Biomedical Research Excellence (INBRE) of the National Institutes of Health [P20RR16475]
  4. Kansas State University
  5. Division of Chemical Sciences of the US Department of Energy [DE-FG02-02ER15295]
  6. U.S. Department of Energy (DOE) [DE-FG02-02ER15295] Funding Source: U.S. Department of Energy (DOE)

向作者/读者索取更多资源

The vacuole is the most prominent compartment in plant cells and is important for ion and protein storage. In our effort to search for key regulators in the plant vacuole sorting pathway, ribosomal large subunit 4 (rpl4d) was identified as a translational mutant defective in both vacuole trafficking and normal development. Polysome profiling of the rpl4d mutant showed reduction in polysome-bound mRNA compared with wild-type, but no significant change in the general mRNA distribution pattern. Ribsomal profiling data indicated that genes in the lipid metabolism pathways were translationally down-regulated in the rpl4d mutant. Live imaging studies by Nile red staining suggested that both polar and nonpolar lipid accumulation was reduced in meristem tissues of rpl4d mutants. Pharmacological evidence showed that sterol and sphingolipid biosynthetic inhibitors can phenocopy the defects of the rpl4d mutant, including an altered vacuole trafficking pattern. Genetic evidence from lipid biosynthetic mutants indicates that alteration in the metabolism of either sterol or sphingolipid biosynthesis resulted in vacuole trafficking defects, similar to the rpl4d mutant. Tissue-specific complementation with key enzymes from lipid biosynthesis pathways can partially rescue both vacuole trafficking and auxin-related developmental defects in the rpl4d mutant. These results indicate that lipid metabolism modulates auxin-mediated tissue differentiation and endomembrane trafficking pathways downstream of ribosomal protein function.

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