| Literature DB >> 34111139 |
Takayuki Hata1,2, Naoto Takada1, Chihiro Hayakawa1, Mei Kazama1, Tomohiro Uchikoba3, Makoto Tachikawa1, Mitsuhiro Matsuo2, Soichirou Satoh1,3, Junichi Obokata2.
Abstract
The manner in which inserted foreign coding sequences become transcriptionally activated and fixed in the plant genome is poorly understood. To examine such processes of gene evolution, we performed an artificial evolutionary experiment in Arabidopsis thaliana. As a model of gene-birth events, we introduced a promoterless coding sequence of the firefly luciferase (LUC) gene and established 386 T2-generation transgenic lines. Among them, we determined the individual LUC insertion loci in 76 lines and found that one-third of them were transcribed de novo even in the intergenic or inherently unexpressed regions. In the transcribed lines, transcription-related chromatin marks were detected across the newly activated transcribed regions. These results agreed with our previous findings in A. thaliana cultured cells under a similar experimental scheme. A comparison of the results of the T2-plant and cultured cell experiments revealed that the de novo-activated transcription concomitant with local chromatin remodelling was inheritable. During one-generation inheritance, it seems likely that the transcription activities of the LUC inserts trapped by the endogenous genes/transcripts became stronger, while those of de novo transcription in the intergenic/untranscribed regions became weaker. These findings may offer a clue for the elucidation of the mechanism by which inserted foreign coding sequences become transcriptionally activated and fixed in the plant genome.Entities:
Year: 2021 PMID: 34111139 DOI: 10.1371/journal.pone.0252674
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240