An optimised method for intact nuclei isolation from diatoms
Autor: | Antonella Ruggiero, Francesco Manfellotto, Maria Immacolata Ferrante, Giovanna Benvenuto, Cecilia Balestra, Rossella Annunziata, Pina Marotta, Elio Biffali |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
0106 biological sciences
0301 basic medicine Lysis Gel electrophoresis of nucleic acids Science Cell Fractionation 01 natural sciences Article Cell wall 03 medical and health sciences Organelle Phaeodactylum tricornutum Fragmentation (cell biology) Cell Nucleus Diatoms Marine biology Microscopy Confocal Multidisciplinary biology Chemistry fungi Functional genomics DNA Chaetoceros diadema biology.organism_classification 030104 developmental biology Diatom Biophysics Medicine Subcellular Fractions 010606 plant biology & botany |
Zdroj: | Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021) Scientific Reports |
ISSN: | 2045-2322 |
Popis: | Due to their abundance in the oceans, their extraordinary biodiversity and the increasing use for biotech applications, the study of diatom biology is receiving more and more attention in the recent years. One of the limitations in developing molecular tools for diatoms lies in the peculiar nature of their cell wall, that is made of silica and organic molecules and that hinders the application of standard methods for cell lysis required, for example, to extract organelles. In this study we present a protocol for intact nuclei isolation from diatoms that was successfully applied to three different species: two pennates, Pseudo-nitzschia multistriata and Phaeodactylum tricornutum, and one centric diatom species, Chaetoceros diadema. Intact nuclei were extracted by treatment with acidified NH4F solution combined to low intensity sonication pulses and separated from cell debris via FAC-sorting upon incubation with SYBR Green. Microscopy observations confirmed the integrity of isolated nuclei and high sensitivity DNA electrophoresis showed that genomic DNA extracted from isolated nuclei has low degree of fragmentation. This protocol has proved to be a flexible and versatile method to obtain intact nuclei preparations from different diatom species and it has the potential to speed up applications such as epigenetic explorations as well as single cell (“single nuclei”) genomics, transcriptomics and proteomics in different diatom species. |
Databáze: | OpenAIRE |
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