Comparative Coexpression Analysis of Indole Synthase and Tryptophan Synthase A Reveals the Independent Production of Auxin via the Cytosolic Free Indole

• Published in: Plants (Basel) 2023-04, Vol.12 (8), p.1687
• Main Authors: Abu-Zaitoon, Yousef M, Al-Ramamneh, Ezz Al-Dein Muhammed, Al Tawaha, Abdel Rahman, Alnaimat, Sulaiman M, Almomani, Fouad A
• Format: Article
• Language: English
• Subjects: Acids; Annotations; Anthranilate synthase; Arabidopsis; Arabidopsis thaliana; Auxin; Auxins; Botanical research; Cell division; coexpression; Comparative analysis; DNA microarrays; Enzymes; Genes; Genetic aspects; Genomes; Genomics; Glycerin; Glycerol; Indole; indole synthase; Indoles; logit score; Phosphates; RNA sequencing; Synthesis; Tryptophan; Tryptophan synthase; tryptophan synthase A; tryptophan synthase B
• ISSN: 2223-7747; 2223-7747
• DOI: 10.3390/plants12081687

Indole synthase (INS), a homologous cytosolic enzyme of the plastidal tryptophan synthase A (TSA), has been reported as the first enzyme in the tryptophan-independent pathway of auxin synthesis. This suggestion was challenged as INS or its free indole product may interact with tryptophan synthase B (TSB) and, therefore, with the tryptophan-dependent pathway. Thus, the main aim of this research was to find out whether INS is involved in the tryptophan-dependent or independent pathway. The gene coexpression approach is widely recognized as an efficient tool to uncover functionally related genes. Coexpression data presented here were supported by both RNAseq and microarray platforms and, hence, considered reliable. Coexpression meta-analyses of Arabidopsis genome was implemented to compare between the coexpression of and with all genes involved in the production of tryptophan via the chorismate pathway. Tryptophan synthase A was found to be coexpressed strongly with , , , as well as . However, was not found to be coexpressed with any target genes suggesting that it may exclusively and independently be involved in the tryptophan-independent pathway. Additionally, annotation of examined genes as ubiquitous or differentially expressed were described and subunits-encoded genes available for the assembly of tryptophan and anthranilate synthase complex were suggested. The most probable TSB subunits expected to interact with TSA is TSB1 then TSB2. Whereas TSB3 is only used under limited hormone conditions to assemble tryptophan synthase complex, putative TSB4 is not expected to be involved in the plastidial synthesis of tryptophan in Arabidopsis.