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.

Highlights

  • Genomes exhibit a steady state of the dynamic activity between the gain and loss of genes

  • To investigate the mechanism of promoter birth and their genetic behaviours beyond one generation, we performed a promoter-trap screening using A. thaliana plants under conditions that were essentially the same as those used in a previous study of cultured cells [26]

  • In this study, based on the large-scale promoter-trap screening of A. thaliana plants, we demonstrated the genetic behaviour of the newly activated transcription of exogenous genes

Read more

Summary

Introduction

Genomes exhibit a steady state of the dynamic activity between the gain and loss of genes. Comparative functional genomics among closely related species revealed how genomes acquired such genetic novelty during their evolution, i.e., duplication–diversification, transposition, gene transfer or de novo origination [1,2,3,4]. To become functional, new coding sequences must acquire promoters during their evolution. Genetic behaviours of de novo transcription collection and analysis, decision to publish, or preparation of the manuscript

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call