Tea,
made from leaves of Camellia sinensis, has
long been consumed worldwide for its unique taste and aroma. Terpenoids
play important roles not only in tea beverage aroma formation, but
also in the productivity and quality of tea plantation due to their
significant contribution to light harvesting pigments and phytohormones.
To date, however, the regulation of terpenoid synthase genes remains
unclear. Herein, the analyses of metabolomics, sRNAs, degradome, and
transcriptomics were performed and integrated for identifying key
regulatory miRNA-target circuits on terpenoid biosynthesis in leaf
tissues over five different months in which the amount of terpenoids
in tea leaves varies greatly. Four classes of miRNA-TF pairs that
might play a central role in the regulation of terpenoid biosynthesis
were also uncovered. Ultimately, a hypothetical model was proposed
that mature miRNAs maintained by light regulator at both the transcriptional
and posttranscriptional levels negatively regulate the targets to
control terpenoid biosynthesis.
Gray blight (GB) is one of the most destructive diseases of tea plants, causing considerable damage and productivity losses; however, the dynamic roles of defense genes during pathogen infection remain largely unclear. To explore the numerous molecular interactions associated with GB stress in tea plants, we employed transcriptome, sRNAome and degradome sequencing from 1 to 13 days post-inoculation (dpi) at 3-day intervals. The transcriptomics results showed that differentially expressed genes (DEGs) related to flavonoid synthesis, such as chalcone synthase (CHS) and phenylalanine ammonia-lyase (PAL), were particularly induced at 4 dpi. Consistent with this, the contents of catechins (especially gallocatechin), which are the dominant flavonoids in tea plants, also increased in the leaves of tea plants infected with GB. Combined analysis of the sRNAome and degradome revealed that microRNAs could mediate tea plant immunity by regulating DEG expression at the post-transcriptional level. Co-expression network analysis demonstrated that miR530b-ethylene responsive factor 96 (ERF96) and miRn211-thaumatin-like protein (TLP) play crucial roles in the response to GB. Accordingly, gene-specific antisense oligonucleotide assays suggested that suppressing ERF96 decreased the levels of reactive oxygen species (ROS), whereas suppressing TLP increased the levels of ROS. Furthermore, ERF96 was induced, but TLP was suppressed, in susceptible tea cultivars. Our results collectively demonstrate that ERF96 is a negative regulator and TLP is a positive regulator in the response of tea plants to GB. Taken together, our comprehensive integrated analysis reveals a dynamic regulatory network linked to GB stress in tea plants and provides candidate genes for improvement of tea plants.
Background: Alternative splicing (AS) may generate multiple mRNA splicing isoforms from a single mRNA precursor using different splicing sites, leading to enhanced diversity of transcripts and proteins. AS has been implicated in cold acclimation by affecting gene expression in various ways, yet little information is known about how AS influences cold responses in tea plant (Camellia sinensis).Results: In this study, the AS transcriptional landscape was characterized in the tea plant genome using highthroughput RNA-seq during cold acclimation. We found that more than 41% (14,103) of genes underwent AS events. We summarize the possible existence of 11 types of AS events, including the four common types of intron retention (IR), exon skipping (ES), alternative 5′ splice site (A5SS), and alternative 3′ splice site (A3SS); of these, IR was the major type in all samples. The number of AS events increased rapidly during cold treatment, but decreased significantly following de-acclimation (DA). It is notable that the number of differential AS genes gradually increased during cold acclimation, and these genes were enriched in pathways relating to oxidoreductase activity and sugar metabolism during acclimation and de-acclimation. Remarkably, the AS isoforms of bHLH transcription factors showed higher expression levels than their full-length ones during cold acclimation. Interestingly, the expression pattern of some AS transcripts of raffinose and sucrose synthase genes were significantly correlated with sugar contents. Conclusion: Our findings demonstrated that changes in AS numbers and transcript expression may contribute to rapid changes in gene expression and metabolite profile during cold acclimation, suggesting that AS events play an important regulatory role in response to cold acclimation in tea plant.
Based
on the abundance of taste compounds in leaves at different
leaf positions on the same shoot, green tea made from one bud and
one leaf, or even just one bud, has the best quality. To elucidate
the mechanism underlying the regulation of the biosynthesis of these
compounds, we profiled the metabolome, transcriptome, sRNA, degradome,
and WGCNA using leaves from five leaf positions of shoots. Through
this analysis, we found 139 miRNA-target pairs related to taste compound
biosynthesis and 96 miRNA-target pairs involved in phytohormone synthesis
or signal transduction. Moreover, miR166-HD-ZIP,
miR169-NF-YA, IAA, ZA, ABA, and JA were positively
related to the accumulation of gallated catechin, caffeine, and theanine.
However, miR396-GRF, miR393-bHLH, miR156-SBP, and SA were negatively correlated
with these compounds. Among these important pairs, the miR396-GRF and miR156-SBP pairs were further validated
by using qRT-PCR, Northern blots, and cotransformation. This is the
first report describing that miRNA-TF pairs and phytohormones might
synergistically regulate the biosynthesis of taste compounds in the
leaves of tea plants.
Gray blight disease, caused by Pestalotiopsis-like fungi, is one of the deadliest threats to tea (Camellia sinensis) production. However, little information is known about the traits and characteristics of this pathogen. Here, a systematic survey was performed, and a total of 20 representative isolates were obtained from the leaves of tea plants affected by gray blight in two main tea plantations located in Anhui Province, China. Further analyses showed that two isolates were identified as Neopestalotiopsis ellipsospora, three isolates were regarded as Pseudopestalotiopsis chinensis, one isolate was considered as Pseudopestalotiopsis camelliae-sinensis, and the remaining isolates belonged to Pseudopestalotiopsis spp., on the basis of morphological characteristics and multigene phylogenetic analyses of the internal transcribed spacer, β-tubulin, and translation elongation factor 1-α. Pathogenicity tests indicated that there were significant differences in virulence among the Neopestalotiopsis and Pseudopestalotiopsis isolates when inoculated on the leaves of the tea plant (C. sinensis ‘Shuchazao’). Furthermore, varied pathogenicity was also observed for the same isolate when inoculated on different varieties of tea plants. To our knowledge, this is the first record of Neopestalotiopsis ellipsospora and Pseudopestalotiopsis chinensis causing gray blight disease of tea plants in China.
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