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Cell Type-Specific Promoters of Volvox carteri for Molecular Cell Biology Studies
The multicellular green alga Volvox carteri has emerged as a valuable model organism for investigating various aspects of multicellularity and cellular differentiation, photoreception and phototaxis, cell division, biogenesis of the extracellular matrix and morphogenetic movements. While a range of...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10379329/ https://www.ncbi.nlm.nih.gov/pubmed/37510294 http://dx.doi.org/10.3390/genes14071389 |
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author | von der Heyde, Benjamin von der Heyde, Eva Laura Hallmann, Armin |
author_facet | von der Heyde, Benjamin von der Heyde, Eva Laura Hallmann, Armin |
author_sort | von der Heyde, Benjamin |
collection | PubMed |
description | The multicellular green alga Volvox carteri has emerged as a valuable model organism for investigating various aspects of multicellularity and cellular differentiation, photoreception and phototaxis, cell division, biogenesis of the extracellular matrix and morphogenetic movements. While a range of molecular tools and bioinformatics resources have been made available for exploring these topics, the establishment of cell type-specific promoters in V. carteri has not been achieved so far. Therefore, here, we conducted a thorough screening of transcriptome data from RNA sequencing analyses of V. carteri in order to identify potential cell type-specific promoters. Eventually, we chose two putative strong and cell type-specific promoters, with one exhibiting specific expression in reproductive cells (gonidia), the PCY1 promoter, and the other in somatic cells, the PFP promoter. After cloning both promoter regions, they were introduced upstream of a luciferase reporter gene. By using particle bombardment, the DNA constructs were stably integrated into the genome of V. carteri. The results of the expression analyses, which were conducted at both the transcript and protein levels, demonstrated that the two promoters drive cell type-specific expression in their respective target cell types. Transformants with considerably diverse expression levels of the chimeric genes were identifiable. In conclusion, the screening and analysis of transcriptome data from RNA sequencing allowed for the identification of potential cell type-specific promoters in V. carteri. Reporter gene constructs demonstrated the actual usability of two promoters. The investigated PCY1 and PFP promoters were proven to be potent molecular tools for genetic engineering in V. carteri. |
format | Online Article Text |
id | pubmed-10379329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103793292023-07-29 Cell Type-Specific Promoters of Volvox carteri for Molecular Cell Biology Studies von der Heyde, Benjamin von der Heyde, Eva Laura Hallmann, Armin Genes (Basel) Article The multicellular green alga Volvox carteri has emerged as a valuable model organism for investigating various aspects of multicellularity and cellular differentiation, photoreception and phototaxis, cell division, biogenesis of the extracellular matrix and morphogenetic movements. While a range of molecular tools and bioinformatics resources have been made available for exploring these topics, the establishment of cell type-specific promoters in V. carteri has not been achieved so far. Therefore, here, we conducted a thorough screening of transcriptome data from RNA sequencing analyses of V. carteri in order to identify potential cell type-specific promoters. Eventually, we chose two putative strong and cell type-specific promoters, with one exhibiting specific expression in reproductive cells (gonidia), the PCY1 promoter, and the other in somatic cells, the PFP promoter. After cloning both promoter regions, they were introduced upstream of a luciferase reporter gene. By using particle bombardment, the DNA constructs were stably integrated into the genome of V. carteri. The results of the expression analyses, which were conducted at both the transcript and protein levels, demonstrated that the two promoters drive cell type-specific expression in their respective target cell types. Transformants with considerably diverse expression levels of the chimeric genes were identifiable. In conclusion, the screening and analysis of transcriptome data from RNA sequencing allowed for the identification of potential cell type-specific promoters in V. carteri. Reporter gene constructs demonstrated the actual usability of two promoters. The investigated PCY1 and PFP promoters were proven to be potent molecular tools for genetic engineering in V. carteri. MDPI 2023-07-01 /pmc/articles/PMC10379329/ /pubmed/37510294 http://dx.doi.org/10.3390/genes14071389 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article von der Heyde, Benjamin von der Heyde, Eva Laura Hallmann, Armin Cell Type-Specific Promoters of Volvox carteri for Molecular Cell Biology Studies |
title | Cell Type-Specific Promoters of Volvox carteri for Molecular Cell Biology Studies |
title_full | Cell Type-Specific Promoters of Volvox carteri for Molecular Cell Biology Studies |
title_fullStr | Cell Type-Specific Promoters of Volvox carteri for Molecular Cell Biology Studies |
title_full_unstemmed | Cell Type-Specific Promoters of Volvox carteri for Molecular Cell Biology Studies |
title_short | Cell Type-Specific Promoters of Volvox carteri for Molecular Cell Biology Studies |
title_sort | cell type-specific promoters of volvox carteri for molecular cell biology studies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10379329/ https://www.ncbi.nlm.nih.gov/pubmed/37510294 http://dx.doi.org/10.3390/genes14071389 |
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