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RNA preservation of Antarctic marine invertebrates

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Abstract

Fifteen species of marine invertebrate commonly occurring in the near-shore environment of Rothera base, Antarctica, were used to test tissue sample storage protocols with regard to preservation of RNA integrity. After animal collection, the tissues were either immediately extracted for RNA or stored at −80°C after having been, either directly flash frozen in liquid nitrogen or preserved in a commercial RNA storage solution, for extraction in the UK. In four cases, direct flash freezing produced enhanced RNA integrity compared with samples in the commercial storage solution. A subset of samples were further tested for the preferred temperature of storage in the commercial reagent. RNA integrity was well preserved at both +4 and −20°C over periods of 2 months, but degradation was rapid in tissues stored at room temperature. Eight out of the fifteen species only produced a single ribosomal band on gel electrophoresis. This survey provides a guide for tissue transport of Polar cold water marine invertebrates.

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Acknowledgments

This paper was produced within the BAS Polar Sciences for Planet Earth Programme; Adaptations and Physiology Work Package. Thanks to all members of the Rothera Dive Team for providing samples and especially to Professor Lloyd Peck for dissecting the Parborlasia. Overall, diving support was provided by the NERC National Facility for Scientific Diving at Oban.

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Correspondence to Melody S. Clark.

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Hillyard, G., Clark, M.S. RNA preservation of Antarctic marine invertebrates. Polar Biol 35, 633–636 (2012). https://doi.org/10.1007/s00300-011-1088-9

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  • DOI: https://doi.org/10.1007/s00300-011-1088-9

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