Seaweeds are essential for marine ecosystems and have immense economic value. Here we present a comprehensive analysis of the draft genome of Saccharina japonica, one of the most economically important seaweeds. The 537-Mb assembled genomic sequence covered 98.5% of the estimated genome, and 18,733 protein-coding genes are predicted and annotated. Gene families related to cell wall synthesis, halogen concentration, development and defence systems were expanded. Functional diversification of the mannuronan C-5-epimerase and haloperoxidase gene families provides insight into the evolutionary adaptation of polysaccharide biosynthesis and iodine antioxidation. Additional sequencing of seven cultivars and nine wild individuals reveal that the genetic diversity within wild populations is greater than among cultivars. All of the cultivars are descendants of a wild S. japonica accession showing limited admixture with S. longissima. This study represents an important advance toward improving yields and economic traits in Saccharina and provides an invaluable resource for plant genome studies.
Salinity is a major and complex abiotic stress that inhibits plant growth and reduces crop yield. Given the global increase in soil salinity, there is a need to develop salt-tolerant species.
Brassica napus
L. is an important oilseed crop with some level of salt tolerance. However, few studies have evaluated its salt tolerance thoroughly or screened for traits that can be reliably evaluated for salt tolerance. Here, we evaluated salt tolerance in 549
B. napus
inbred lines with different genetic backgrounds using the membership function value (MFV) of certain traits, including the germination rate, root and shoot length, root and shoot fresh weight, and total fresh weight. According to the evaluation criteria-mean MFV, 50 highly salt-tolerant, 115 salt-tolerant, 71 moderately salt-tolerant, 202 salt-sensitive, and 111 highly salt-sensitive inbred lines were screened at the germination stage. We also developed a mathematical evaluation model and identified that the salt tolerance index of shoot fresh weight is a single trait that reliably represents the salt tolerance of
B. napus
germplasm at the germination stage. These results are useful for evaluating and breeding salt-tolerant
B. napus
germplasm.
Quantitative real-time reverse transcription PCR (qRT-PCR), a sensitive technique for quantifying gene expression, depends on the stability of the reference gene(s) used for data normalization. Only a few studies on the reference genes have been done with peanut to date. In the present study, 14 potential reference genes in peanut were evaluated for their expression stability using the geNorm and NormFinder statistical algorithms. Expression stability was assessed by qRT-PCR across 32 biological samples, including various tissue types, seed developmental stages, salt and cold treatments. The results showed that the best-ranked references genes differed across the samples. UKN1, UKN2, TUA5 and ACT11 were the most stable across all the tested samples. A combination of ACT11, TUA5, UKN2, PEPKR1 and TIP41 would be appropriate as a reference panel for normalizing gene expression data across the various tissues tested, whereas the combination of TUA5 and UKN1 was the most suitable for seed developmental stages. TUA5 and EF1b exhibited the most stable expression under cold treatment. For salt-treated leaves, TUA5 and UKN2 were the most stably expressed and HDC and UKN1 for salt-treated roots. The relative gene expression level of peanut Cys(2)/His(2)-type zinc finger protein gene AhZFP1 was analyzed in order to validate the reference genes selected for this study. These results provide guidelines for the selection of reference genes under different experimental conditions and also a foundation for more accurate and widespread use of qRT-PCR in peanut gene analysis.
Summary
Brown algae have convergently evolved plant‐like body plans and reproductive cycles, which in plants are controlled by differential DNA methylation. This contribution provides the first single‐base methylome profiles of haploid gametophytes and diploid sporophytes of a multicellular alga.
Although only c. 1.4% of cytosines in Saccharina japonica were methylated mainly at CHH sites and characterized by 5‐methylcytosine (5mC), there were significant differences between life‐cycle stages. DNA methyltransferase 2 (DNMT2), known to efficiently catalyze tRNA methylation, is assumed to methylate the genome of S. japonica in the structural context of tRNAs as the genome does not encode any other DNA methyltransferases. Circular and long noncoding RNA genes were the most strongly methylated regulatory elements in S. japonica.
Differential expression of genes was negatively correlated with DNA methylation with the highest methylation levels measured in both haploid gametophytes. Hypomethylated and highly expressed genes in diploid sporophytes included genes involved in morphogenesis and halogen metabolism.
The data herein provide evidence that cytosine methylation, although occurring at a low level, is significantly contributing to the formation of different life‐cycle stages, tissue differentiation and metabolism in brown algae.
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