Identifying transcription factors involved in Arabidopsis adventious shoot regeneration by RNA-Seq technology.
- Author:
Xingchun WANG
;
Zhao CHEN
;
Juan FAN
;
Miaomiao HE
;
Yuanhuai HAN
;
Zhirong YANG
- Publication Type:Journal Article
- MeSH:
Arabidopsis;
growth & development;
Arabidopsis Proteins;
physiology;
Gene Expression Regulation, Plant;
Genes, Plant;
Plant Shoots;
growth & development;
RNA;
Regeneration;
Seedlings;
growth & development;
Transcription Factors;
physiology;
Up-Regulation
- From:
Chinese Journal of Biotechnology
2015;31(4):552-565
- CountryChina
- Language:Chinese
-
Abstract:
Transcriptional regulation is one of the major regulations in plant adventious shoot regeneration, but the exact mechanism remains unclear. In our study, the RNA-seq technology based on the IlluminaHiSeq 2000 sequencing platform was used to identify differentially expressed transcription factor (TF) encoding genes during callus formation stage and adventious shoot regeneration stage between wild type and adventious shoot formation defective mutant be1-3 and during the transition from dedifferentiation to redifferentiation stage in wildtype WS. Results show that 155 TFs were differentially expressed between be1-3 mutant and wild type during callus formation, of which 97 genes were up-regulated, and 58 genes were down-regulated; and that 68 genes were differentially expressed during redifferentiation stage, with 40 genes up-regulated and 28 genes down-regulated; whereas at the transition stage from dedifferentiation to redifferention in WS wild type explants, a total of 231 differentially expressed TF genes were identified, including 160 up-regualted genes and 71 down-regulated genes. Among these TF genes, the adventious shoot related transcription factor 1 (ART1) gene encoding a MYB-related (v-myb avian myeloblastosis viral oncogene homolog) TF, was up-regulated 3 217 folds, and was the highest up-regulated gene during be1-3 callus formation. Over expression of the ART1 gene caused defects in callus formation and shoot regeneration and inhibited seedling growth, indicating that the ART1 gene is a negative regulator of callus formation and shoot regeneration. This work not only enriches our knowledge about the transcriptional regulation mechanism of adventious shoot regeneration, but also provides valuable information on candidate TF genes associated with adventious shoot regeneration for future research.
