Abstract

Deoxycytidine monophosphate deaminase (DCD) is a key enzyme in the de novo dTTP biosynthesis pathway. Previous studies have indicated that DCD plays key roles in the maintenance of the balance of dNTP pools, cell cycle progression, and plant development. However, few studies have elucidated the functions of the DCD gene in Panicoideae plants. Setaria has been proposed as an ideal model of Panicoideae grasses, especially for C4 photosynthesis research. Here, a Setaria italica stripe leaf mutant (sistl2) was isolated from EMS-induced lines of “Yugu1,” the wild-type parent. The sistl2 mutant exhibited semi-dwarf, striped leaves, abnormal chloroplast ultrastructure, and delayed cell cycle progression compared with Yugu1. High-throughput sequencing and map-based cloning identified the causal gene SiSTL2, which encodes a DCD protein. The occurrence of a single-base G to A substitution in the fifth intron introduced alternative splicing, which led to the early termination of translation. Further physiological and transcriptomic investigation indicated that SiSTL2 plays an essential role in the regulation of chloroplast biogenesis, cell cycle, and DNA replication, which suggested that the gene has conserved functions in both foxtail millet and rice. Remarkably, in contrast to DCD mutants in C3 rice, sistl2 showed a significant reduction in leaf cell size and affected C4 photosynthetic capacity in foxtail millet. qPCR showed that SiSTL2 had a similar expression pattern to typical C4 genes in response to a low CO2 environment. Moreover, the loss of function of SiSTL2 resulted in a reduction of leaf 13C content and the enrichment of DEGs in photosynthetic carbon fixation. Our research provides in-depth knowledge of the role of DCD in the C4 photosynthesis model S. italica and proposed new directions for further study of the function of DCD.

Highlights

  • Deoxycytidine monophosphate deaminase (DCD) is a key enzyme in the de novo deoxythymidine triphosphate synthesis pathway

  • These results indicated that leaf extension and reproductive development were impaired in sistl2

  • The results showed that the expression of salvage pathway genes in the mutant was decreased. These results suggested that the mutation in SiSTL2 influenced both the de novo pathway and the salvage pathway of deoxythymidine triphosphate (dTTP) biosynthesis

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Summary

Introduction

Deoxycytidine monophosphate deaminase (DCD) is a key enzyme in the de novo deoxythymidine triphosphate (dTTP) synthesis pathway. DTTP and deoxycytidine triphosphate (dCTP) are the inhibitor and activator of DCD, respectively, which competitively bind to the allosteric site to control protein stability and further regulate the activity of DCD (Hou et al, 2008; Marx and Alian, 2015) This allosteric regulation depends on the participation of divalent metal ions, such as Ca2+ and Mg2+ (Scortecci et al, 2017). When either of the de novo or salvage pathway is defective, the other can compensate for the loss of pyrimidine synthesis function (Leija et al, 2016) These pathways are mutually interrelated to maintain sufficient dTTP and the balance of the dNTP pools. The biosynthesis of dTTP is a highly coordinated process

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