The GluTR-binding protein is the heme-binding factor for feedback control of glutamyl-tRNA reductase.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 31194674.
- Also identified by DOI 10.7554/eLife.46300 and PMC identifier 6597238.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Synthesis of 5-aminolevulinic acid (ALA) is the rate-limiting step in tetrapyrrole biosynthesis in land plants. In photosynthetic eukaryotes and many bacteria, glutamyl-tRNA reductase (GluTR) is the most tightly controlled enzyme upstream of ALA. Higher plants possess two GluTR isoforms: GluTR1 is predominantly expressed in green tissue, and GluTR2 is constitutively expressed in all organs. Although proposed long time ago, the molecular mechanism of heme-dependent inhibition of GluTR <i>in planta</i> has remained elusive. Here, we report that accumulation of heme, induced by feeding with ALA, stimulates Clp-protease-dependent degradation of <i>Arabidopsis</i> GluTR1. We demonstrate that binding of heme to the GluTR-binding protein (GBP) inhibits interaction of GBP with the N-terminal regulatory domain of GluTR1, thus making it accessible to the Clp protease. The results presented uncover a functional link between heme content and the post-translational control of GluTR stability, which helps to ensure adequate availability of chlorophyll and heme.
Medical subject headings
- Aldehyde Oxidoreductases
- Arabidopsis
- Arabidopsis Proteins
- Carrier Proteins
- Feedback, Physiological
- Heme