Cargando…
Transcriptome Analysis in Yeast Reveals the Externality of Position Effects
The activity of a gene newly integrated into a chromosome depends on the genomic context of the integration site. This “position effect” has been widely reported, although the other side of the coin, that is, how integration affects the local chromosomal environment, has remained largely unexplored,...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321525/ https://www.ncbi.nlm.nih.gov/pubmed/33871622 http://dx.doi.org/10.1093/molbev/msab104 |
_version_ | 1783730871196450816 |
---|---|
author | Gui, Qian Deng, Shuyun Zhou, ZhenZhen Cao, Waifang Zhang, Xin Shi, Wenjun Cai, Xiujuan Jiang, Wenbing Cui, Zifeng Hu, Zheng Chen, Xiaoshu |
author_facet | Gui, Qian Deng, Shuyun Zhou, ZhenZhen Cao, Waifang Zhang, Xin Shi, Wenjun Cai, Xiujuan Jiang, Wenbing Cui, Zifeng Hu, Zheng Chen, Xiaoshu |
author_sort | Gui, Qian |
collection | PubMed |
description | The activity of a gene newly integrated into a chromosome depends on the genomic context of the integration site. This “position effect” has been widely reported, although the other side of the coin, that is, how integration affects the local chromosomal environment, has remained largely unexplored, as have the mechanism and phenotypic consequences of this “externality” of the position effect. Here, we examined the transcriptome profiles of approximately 250 Saccharomyces cerevisiae strains, each with GFP integrated into a different locus of the wild-type strain. We found that in genomic regions enriched in essential genes, GFP expression tended to be lower, and the genes near the integration site tended to show greater expression reduction. Further joint analysis with public genome-wide histone modification profiles indicated that this effect was associated with H3K4me2. More importantly, we found that changes in the expression of neighboring genes, but not GFP expression, significantly altered the cellular growth rate. As a result, genomic loci that showed high GFP expression immediately after integration were associated with growth disadvantages caused by elevated expression of neighboring genes, ultimately leading to a low total yield of GFP in the long run. Our results were consistent with competition for transcriptional resources among neighboring genes and revealed a previously unappreciated facet of position effects. This study highlights the impact of position effects on the fate of exogenous gene integration and has significant implications for biological engineering and the pathology of viral integration into the host genome. |
format | Online Article Text |
id | pubmed-8321525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83215252021-07-30 Transcriptome Analysis in Yeast Reveals the Externality of Position Effects Gui, Qian Deng, Shuyun Zhou, ZhenZhen Cao, Waifang Zhang, Xin Shi, Wenjun Cai, Xiujuan Jiang, Wenbing Cui, Zifeng Hu, Zheng Chen, Xiaoshu Mol Biol Evol Discoveries The activity of a gene newly integrated into a chromosome depends on the genomic context of the integration site. This “position effect” has been widely reported, although the other side of the coin, that is, how integration affects the local chromosomal environment, has remained largely unexplored, as have the mechanism and phenotypic consequences of this “externality” of the position effect. Here, we examined the transcriptome profiles of approximately 250 Saccharomyces cerevisiae strains, each with GFP integrated into a different locus of the wild-type strain. We found that in genomic regions enriched in essential genes, GFP expression tended to be lower, and the genes near the integration site tended to show greater expression reduction. Further joint analysis with public genome-wide histone modification profiles indicated that this effect was associated with H3K4me2. More importantly, we found that changes in the expression of neighboring genes, but not GFP expression, significantly altered the cellular growth rate. As a result, genomic loci that showed high GFP expression immediately after integration were associated with growth disadvantages caused by elevated expression of neighboring genes, ultimately leading to a low total yield of GFP in the long run. Our results were consistent with competition for transcriptional resources among neighboring genes and revealed a previously unappreciated facet of position effects. This study highlights the impact of position effects on the fate of exogenous gene integration and has significant implications for biological engineering and the pathology of viral integration into the host genome. Oxford University Press 2021-04-19 /pmc/articles/PMC8321525/ /pubmed/33871622 http://dx.doi.org/10.1093/molbev/msab104 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Discoveries Gui, Qian Deng, Shuyun Zhou, ZhenZhen Cao, Waifang Zhang, Xin Shi, Wenjun Cai, Xiujuan Jiang, Wenbing Cui, Zifeng Hu, Zheng Chen, Xiaoshu Transcriptome Analysis in Yeast Reveals the Externality of Position Effects |
title | Transcriptome Analysis in Yeast Reveals the Externality of Position Effects |
title_full | Transcriptome Analysis in Yeast Reveals the Externality of Position Effects |
title_fullStr | Transcriptome Analysis in Yeast Reveals the Externality of Position Effects |
title_full_unstemmed | Transcriptome Analysis in Yeast Reveals the Externality of Position Effects |
title_short | Transcriptome Analysis in Yeast Reveals the Externality of Position Effects |
title_sort | transcriptome analysis in yeast reveals the externality of position effects |
topic | Discoveries |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321525/ https://www.ncbi.nlm.nih.gov/pubmed/33871622 http://dx.doi.org/10.1093/molbev/msab104 |
work_keys_str_mv | AT guiqian transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects AT dengshuyun transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects AT zhouzhenzhen transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects AT caowaifang transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects AT zhangxin transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects AT shiwenjun transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects AT caixiujuan transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects AT jiangwenbing transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects AT cuizifeng transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects AT huzheng transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects AT chenxiaoshu transcriptomeanalysisinyeastrevealstheexternalityofpositioneffects |