Transcriptomic response to cold of thermophilous medicinal plant Marsdenia tenacissima

•Cold is one of factors restrain the domesticated cultivation of M. tenacissima.•How M. tenacissima response to cold stress has never been investigated.•Cold responsive genes abundant with transcription factors and secondary metabolism.•MtEF1α worked as the best internal control across developmental...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Gene 2020-06, Vol.742, p.144602-144602, Article 144602
Hauptverfasser: Long, Guangqiang, Zhao, Changhong, Zhao, Ping, Zhou, Chengli, Ntirenganya, Elie, Zhou, Yanli
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•Cold is one of factors restrain the domesticated cultivation of M. tenacissima.•How M. tenacissima response to cold stress has never been investigated.•Cold responsive genes abundant with transcription factors and secondary metabolism.•MtEF1α worked as the best internal control across developmental stage and cold stress.•MYB60 is potentially be a candidate gene for improving cold tolerance and bioactive constituents. Extracts from Marsdenia tenacissima, involving tenacissoside H, I and G, have been used as remedies of cancer, inflammation and asthma. Low temperature serves as one of the main factors constrain the planting expansion and quality of M. tenacissima, but its functional mechanism has been known scarcely for the lack of genomic information and transcriptional profile. Here we investigated the transcriptomic responses of M. tenacissima under cold stress to gain insight into the molecular mechanism of low temperature sensitivity. Total RNAs were collected from samples obtained at 4-time points (after 0, 3, 6 and 48 h cold treatments with 4 °C, respectively), then used for library construction and sequenced on the Illumina Hiseq™ 4000 platform. Passing quality assessments, 500794 transcripts, and 206137 unigenes were de novo assembly out in Trinity v2.4.0, holding contig N50 of 2566 bp and unigene mean length of 754 bp. 44.20% of assembled unigenes were annotated to the well-known public protein database on a basis of sequence similarity. Using statistical comparison of the fragments per kilo base of transcript per million reads mapped (FPKM) values between conditions, 6082 group-specific differentially expressed genes (DEGs) were identified and considered as cold-responsive genes, which contained copious transcription factors and active secondary metabolism. Among them, 43 unigenes were constantly up-regulated expression along with cold time, which mainly implicated in the biosynthesis of secondary metabolites, carbon metabolism, RNA and DNA metabolism. Conversely, 21 unigenes involved in photosynthesis, cell wall, protein degradation, and transporters were downregulated continually with cold timescale. Experimentally, MtEF1α was chosen as the best housekeeping gene. Functional enrichments found that damaging of cold stress on M. tenacissima may be ascribed to inability of photosynthesis, ribsome processing, flavonoid biosynthesis and terpenoids degradation. Correlation analysis between cold induced transcription factors and tenacissoside biosynth
ISSN:0378-1119
1879-0038
DOI:10.1016/j.gene.2020.144602