Analysis of T-DNA integration events in transgenic rice

Copyright © 2021 Elsevier GmbH. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Journal of plant physiology. - 1979. - 266(2021) vom: 15. Nov., Seite 153527
1. Verfasser: Gong, Wankui (VerfasserIn)
Weitere Verfasser: Zhou, Yun, Wang, Rui, Wei, Xiaoli, Zhang, Lei, Dai, Yan, Zhu, Zhen
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2021
Zugriff auf das übergeordnete Werk:Journal of plant physiology
Schlagworte:Journal Article Cut/paste mechanism Filler DNA Microhomology T-DNA integration Transgenic rice Translocation DNA, Bacterial DNA, Plant T-DNA
Beschreibung
Zusammenfassung:Copyright © 2021 Elsevier GmbH. All rights reserved.
Agrobacterium-mediated plant transformation has been widely used for introducing transgene(s) into a plant genome and plant breeding. However, our understanding of T-DNA integration into rice genome remains limited relative to that in the model dicot Arabidopsis. To better elucidate the T-DNA integration into the rice genome, we investigated extensively the T-DNA ends and their flanking rice genomic sequences from two transgenic rice plants carrying Cowpea Trypsin Inhibitor (CpTI)-derived gene Signal-CpTI-KDEL (SCK) and Bacillus thuringiensis (BT) gene, respectively, by TAIL-PCR method. Analysis of the junction sequences between the T-DNA ends and rice genome DNA indicated that there were three joining patterns of microhomology, filler DNA sequences, and exact joining, and both the T-DNA ends tend to adopt identical manner to join the rice genome. After T-DNA integration, there were several variations of rice genomic sequences, including small deletions at the integration sites, superfluous DNA inserted between T-DNA and genome, and translocation of genomic DNA in the flanking regions. The translocation block could be from a noncontiguous region in the same chromosome or different chromosomes at the integration sites, and the originating position of the translocated block resulted in comparable deletion based on a cut/paste mechanism rather than a replication mechanism. Our study may lead to a better understand of T-DNA integration mechanism and facilitate functional genomic studies and further crop improvement
Beschreibung:Date Completed 13.01.2022
Date Revised 13.01.2022
published: Print-Electronic
Citation Status MEDLINE
ISSN:1618-1328
DOI:10.1016/j.jplph.2021.153527