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. 2016 Sep;67(17):5105-17.
doi: 10.1093/jxb/erw275. Epub 2016 Jul 19.

Systems analysis of cis-regulatory motifs in C4 photosynthesis genes using maize and rice leaf transcriptomic data during a process of de-etiolation

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Systems analysis of cis-regulatory motifs in C4 photosynthesis genes using maize and rice leaf transcriptomic data during a process of de-etiolation

Jiajia Xu et al. J Exp Bot. 2016 Sep.

Erratum in

  • Corrigendum.
    Xu J, Bräutigam A, Li Y, Weber APM, Zhu XG. Xu J, et al. J Exp Bot. 2017 May 17;68(11):3035. doi: 10.1093/jxb/erw461. J Exp Bot. 2017. PMID: 28007949 Free PMC article. No abstract available.

Abstract

Identification of potential cis-regulatory motifs controlling the development of C4 photosynthesis is a major focus of current research. In this study, we used time-series RNA-seq data collected from etiolated maize and rice leaf tissues sampled during a de-etiolation process to systematically characterize the expression patterns of C4-related genes and to further identify potential cis elements in five different genomic regions (i.e. promoter, 5'UTR, 3'UTR, intron, and coding sequence) of C4 orthologous genes. The results demonstrate that although most of the C4 genes show similar expression patterns, a number of them, including chloroplast dicarboxylate transporter 1, aspartate aminotransferase, and triose phosphate transporter, show shifted expression patterns compared with their C3 counterparts. A number of conserved short DNA motifs between maize C4 genes and their rice orthologous genes were identified not only in the promoter, 5'UTR, 3'UTR, and coding sequences, but also in the introns of core C4 genes. We also identified cis-regulatory motifs that exist in maize C4 genes and also in genes showing similar expression patterns as maize C4 genes but that do not exist in rice C3 orthologs, suggesting a possible recruitment of pre-existing cis-elements from genes unrelated to C4 photosynthesis into C4 photosynthesis genes during C4 evolution.

Keywords: C4 photosynthesis; cell specificity; cis element; etiolation; evolution; systems biology..

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Figures

Fig 1.
Fig 1.
Pathway-level gene expression of maize and rice during the de-etiolation process. The dot size represents the gene expression level across the whole genome. The color code indicates the relative gene expression level within a given pathway, from low (yellow) to high (red). (A) Photosynthetic pathways, and (B) non-photosynthesis related pathways. CCM, CO2 concentration mechanism.
Fig 2.
Fig 2.
Expression curves of C4 gene families. The x-axis represents different time points and the y-axis represents the RPKM value. Expression curves were 3rd-order polynomial regressed, whilst points indicate actual RPKM values.
Fig 3.
Fig 3.
Expression patterns of C4 orthologous gene pairs between maize (red) and rice (blue). RPKM values were normalized after 3rd-order polynomial regression.
Fig 4.
Fig 4.
Diagram showing numbers and species of conserved DNA motifs between maize and rice. Conserved DNA motifs identified with the k80 appraoch are marked with color as indicated in the keys, and the number of mapped sites are shown. Overlapping results between the k80 and k30 approaches are marked in bold in the keys.
Fig 5.
Fig 5.
The number of recruited motif sites in different segments of C4 genes. The total number of mapped sites for potential recruited motifs in maize identified using the k80 approach are given in the corresponding genomic segments, and the number of overlapping motifs is indicated in brackets.

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References

    1. Ali S, Taylor WC. 2001. Quantitative regulation of the Flaveria Me1 gene is controlled by the 3′-untranslated region and sequences near the amino terminus. Plant Molecular Biology 46, 251–261. - PubMed
    1. Aubry S, Brown NJ, Hibberd JM. 2011. The role of proteins in C3 plants prior to their recruitment into the C4 pathway. Journal of Experimental Botany 62, 3049–3059. - PubMed
    1. Aubry S, Smith-Unna RD, Boursnell CM, Kopriva S, Hibberd JM. 2014. Transcript residency on ribosomes reveals a key role for the Arabidopsis thaliana bundle sheath in sulfur and glucosinolate metabolism. Plant Journal 78, 659–673. - PubMed
    1. Bailey TL, Williams N, Misleh C, Li WW. 2006. MEME: discovering and analyzing DNA and protein sequence motifs. Nucleic Acids Research, 34, W369–W373. - PMC - PubMed
    1. Blanchette M. 2003. FootPrinter: a program designed for phylogenetic footprinting. Nucleic Acids Research 31, 3840–3842. - PMC - PubMed

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