Gene mapping and functional analysis of the novel leaf color gene SiYGL1 in foxtail millet [Setaria italica (L.) P. Beauv]
Setaria italica and its wild ancestor Setaria viridis are emerging as model systems for genetics and functional genomics research. However, few systematic gene mapping or functional analyses have been reported in these promising C4 models. We herein isolated the yellow‐green leaf mutant (siygl1) in...
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Published in | Physiologia plantarum Vol. 157; no. 1; pp. 24 - 37 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.05.2016
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Setaria italica and its wild ancestor Setaria viridis are emerging as model systems for genetics and functional genomics research. However, few systematic gene mapping or functional analyses have been reported in these promising C4 models. We herein isolated the yellow‐green leaf mutant (siygl1) in S. italica using forward genetics approaches. Map‐based cloning revealed that SiYGL1, which is a recessive nuclear gene encoding a magnesium‐chelatase D subunit (CHLD), is responsible for the mutant phenotype. A single Phe to Leu amino acid change occurring near the ATPase‐conserved domain resulted in decreased chlorophyll (Chl) accumulation and modified chloroplast ultrastructure. However, the mutation enhanced the light‐use efficiency of the siygl1 mutant, suggesting that the mutated CHLD protein does not completely lose its original activity, but instead, gains novel features. A transcriptional analysis of Chl a oxygenase revealed that there is a strong negative feedback control of Chl b biosynthesis in S. italica. The SiYGL1 mRNA was expressed in all examined tissues, with higher expression observed in the leaves. Comparison of gene expression profiles in wild‐type and siygl1 mutant plants indicated that SiYGL1 regulates a subset of genes involved in photosynthesis (rbcL and LHCB1), thylakoid development (DEG2) and chloroplast signaling (SRP54CP). These results provide information regarding the mutant phenotype at the transcriptional level. This study demonstrated that the genetic material of a Setaria species could be ideal for gene discovery investigations using forward genetics approaches and may help to explain the molecular mechanisms associated with leaf color variation. |
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Bibliography: | The Agricultural Science and Technology Innovation Program of CAAS ark:/67375/WNG-MXQZDGP6-N Fig. S1. Comparative analysis of the amino acid sequences of CHLD proteins in different plant species. The amino acid substitution of CHLD proteins were identified in 10 plant species (Oryza sativa, Zea mays, Setaria italica, Sorghum bicolor, Brachypodium distachyon, Panicum virgatum, Hordeum vulgare, Populus trichocarpa, Glycine max and Arabidopsis thaliana) using HMMER-InterProScan approach. Red arrows stand for the positions of specific mutated amino acids resulting from different alleles in different species.Table S1. Primers designed for map-based cloning. Table S2. Primers used in qRT-PCR analysis. Table S3. Photosynthetic indicators for the siygl1 mutant. SES, stem elongation stage; HS, heading stage; Pn, net photosynthesis rate (µmol m−2 s−1); Gs, stomatal conductance (mol m−2 s−1); Ci, concentration of intercellular CO2 (µmol CO2 mol-1); Tr, transpiration rate (µmol m−2 s−1); Fv/Fm: the primary light energy conversion of PSII; qP: photochemical quenching coefficient; qN, non-photochemical quenching; ΦPSII, quantum yield of photosystem II electron transport; ETR, apparent photosynthetic electron transport rate. Each condition included measurements for three plants, with three measurements per plant. Asterisks indicate a significant difference between siygl1 and Yugu1 plants: n = 9 leaves, Welch's two-sample t-test, P < 0.05. Table S4. Segregation of F1 and F2 populations from two crosses. Table S5. Information for genes located in the candidate region. National Natural Science Foundation of China - No. 31301328; No. 31171560 ArticleID:PPL12405 Chinese Academy of Agricultural Sciences - No. 2014ZL002 Fundamental Research Funds of ICS-CAAS - No. 2013007 China Agricultural Research System - No. CARS07-12.5-A02 Beijing Natural Science Foundation - No. 6142019 istex:7D7D9A02D40713B176CBDEC4560516FAF80D7CCC National High Technology Research and Development Program of China (863 Program) - No. 2013AA102603 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0031-9317 1399-3054 |
DOI: | 10.1111/ppl.12405 |