Full-length transcriptome sequences and the identification of putative genes for flavonoid biosynthesis in safflower
Autor: | Bin Wei, Jiang Chen, Yi-Yun Wu, Chaoxiang Ren, Xiaohui Tang, Qinghua Wu, Jin Pei |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0106 biological sciences
0301 basic medicine Flavonoid biosynthesis PacBio RS II lcsh:QH426-470 lcsh:Biotechnology Flavonoid Carthamus tinctorius Computational biology Cyclopentanes Acetates Proteomics Genes Plant 01 natural sciences Safflower Transcriptome 03 medical and health sciences lcsh:TP248.13-248.65 Gene expression Genetics Oxylipins MeJA treatment Gene chemistry.chemical_classification Flavonoids biology Sequence Analysis RNA Gene Expression Profiling fungi Carthamus food and beverages biology.organism_classification Biosynthetic Pathways lcsh:Genetics 030104 developmental biology Gene Ontology chemistry Full-length transcriptome RNA Long Noncoding DNA microarray 010606 plant biology & botany Biotechnology Microsatellite Repeats Research Article |
Zdroj: | BMC Genomics, Vol 19, Iss 1, Pp 1-13 (2018) BMC Genomics |
ISSN: | 1471-2164 |
Popis: | Background The flower of the safflower (Carthamus tinctorius L.) has been widely used in traditional Chinese medicine for the ability to improve cerebral blood flow. Flavonoids are the primary bioactive components in safflower, and their biosynthesis has attracted widespread interest. Previous studies mostly used second-generation sequencing platforms to survey the putative flavonoid biosynthesis genes. For a better understanding of transcription data and the putative genes involved in flavonoid biosynthesis in safflower, we carry our study. Results High-quality RNA was extracted from six types of safflower tissue. The RNAs of different tissues were mixed equally and used for multiple size-fractionated libraries (1–2, 2–3 and 3-6 k) library construction. Five cells were carried (2 cells for 1–2 and for 2-3 k libraries and 1 cell for 3-6 k libraries). 10.43Gb clean data and 38,302 de-redundant sequences were captured. 44 unique isoforms were annotated as encoding enzymes involved in flavonoid biosynthesis. The full length flavonoid genes were characterized and their evolutional relationship and expressional pattern were analyzed. They can be divided into eight families, with a large differences in the tissue expression. The temporal expressions under MeJA treatment were also measured, 9 genes are significantly up-regulated and 2 genes are significantly down-regulated. The genes involved in flavonoid synthesis in safflower were predicted in our study. Besides, the SSR and lncRNA are also analyzed in our study. Conclusions Full-length transcriptome sequences were used in our study. The genes involved in flavonoid synthesis in safflower were predicted in our study. Combined the determination of flavonoids, CtC4H2, CtCHS3, CtCHI3, CtF3H3, CtF3H1 are mainly participated in MeJA promoting the synthesis of flavonoids. Our results also provide a valuable resource for further study on safflower. Electronic supplementary material The online version of this article (10.1186/s12864-018-4946-9) contains supplementary material, which is available to authorized users. |
Databáze: | OpenAIRE |
Externí odkaz: | |
Nepřihlášeným uživatelům se plný text nezobrazuje | K zobrazení výsledku je třeba se přihlásit. |