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Mager, S.

Publications and source records attributed to Mager, S..

2 recordsLinked to original sources

The genetic basis of dynamic non-photochemical quenching and photosystem II efficiency in fluctuating light reveals novel molecular targets for maize (Zea mays) improvement

Maize (Zea mays L.) is a major global crop species which uses C4 photosynthesis. Although C4 is typically considered to be more efficient than C3 photosynthesis, especially under warmer and drier conditions, there is substantial evidence that its efficiency can still be further improved, which may benefit crop performance. Improving photosynthetic efficiency via targeted manipulation of non-photochemical quenching has focused on a limited set of genes that are known to be important determinants of the NPQ response in C3 plants. The C4 pathway may alter NPQ responses but only relatively few studies have explored genetic variation in NPQ kinetics in species that perform C4 photosynthesis. In addition, studies of NPQ responses in field-grown plants of either C3 or C4 species are especially limited. Here we apply high-definition phenotyping of NPQ responses and photosynthetic efficiency and quantitative trait locus (QTL) mapping using a field-grown maize Multi-parent Advanced Generation Inter-Cross (MAGIC) population, which combines the allelic diversity of eight contrasting inbred lines. We find substantial and consistent variation for dynamic NPQ and PSII efficiency for two subsequent field seasons. Further exploration of candidate genes within three major QTL regions identified a strong impact of allelic variation in expression of the minor PSII antenna protein CP24 (LHCB6) on a major QTL for NPQ and efficiency of PSII photochemistry on chromosome 10.

plant biology↗

DNA methylation is linked to the monoallelic expression of MRP3, a diatom mating type determining gene

Diatoms are unicellular microalgae widely distributed in aquatic ecosystems. In diatoms, sexual reproduction is needed to counteract cell miniaturization imposed by the rigid silica shell, and only small cells, below a species-specific size threshold, are competent for sex. We performed a genome-wide Enzymatic Methyl-seq analysis in the heterothallic diatom Pseudo-nitzschia multistriata comparing cells of different size and opposite mating type (MT) to investigate potential epigenetic controls in life cycle transitions. We found an imprinting-like pattern of methylation at the sex locus: alleles of the gene responsible for the specification of the MT+, MRP3, are hypermethylated in MT- and differentially methylated in MT+, with transcription occurring only on the MT+ hypomethylated variant. The methylation pattern is overall stable over the P. multistriata life cycle. Absence of methylation in MRP3 is necessary for its expression but not sufficient, since large non-sexual cells have the same methylation profile of small sexual cells but do not express MRP3, suggesting that additional controls are involved in the mechanism of sex determination. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=166 SRC="FIGDIR/small/561864v1_ufig1.gif" ALT="Figure 1"> View larger version (29K): org.highwire.dtl.DTLVardef@ea2482org.highwire.dtl.DTLVardef@2d553org.highwire.dtl.DTLVardef@350aaorg.highwire.dtl.DTLVardef@1a4f2f6_HPS_FORMAT_FIGEXP M_FIG C_FIG The methylation profile of the mating type determining gene MRP3 of the diatom Pseudo-nitzschia multistriata is different between opposite mating types. Lack of methylation is necessary but not sufficient for MRP3 expression in the sexually competent MT+ strains. HighlightsO_LI- The mating type locus is differentially methylated in MT+ and MT- C_LIO_LI- DNA methylation is linked to MRP3 expression C_LIO_LI- DNA methylation does not play a role in the acquisition of sexual competence C_LI

genetics↗