Comparison of Different Dna Preservation Methods On Quinqueloculina Spp. (foraminifera, Miliolida)

Author:

Lyu Man12,Lei Yanli12,Li Tiegang324

Affiliation:

1. Laboratory of Marine Organism Taxonomy and Phylogeny, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China

2. University of Chinese Academy of Sciences, Beijing 100049, China

3. Key Laboratory of Marine Sedimentology and Environmental Geology, First Institute of Oceanography, SOA, Qingdao 266061, China

4. Laboratory for Marine Geology, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266061, China

Abstract

Abstract We carried out a series of experiments to evaluate the efficiency of preserving DNA from porcelaneous foraminifera (Quinqueloculina spp.) and a second set to assess the effect of Rose Bengal staining on molecular processing. The first experimental setup assessed three methods of DNA preservation (air-drying, freezing with or without seawater, and Guanidine lysis buffer treatment with or without EDTA (Ethylenediaminetetraacetic acid)). Our study produced the following results: 1) there were no significant differences in DNA preservation when samples were air dried across a range of temperatures (20–120°C); samples frozen at −20°C appeared better preserved than at those frozen at –80°C, and freezing without seawater appeared to produce better preservation than with seawater, though differences in freezing treatments were not significant (p > 0.05); samples in Guanidine lysis buffer with EDTA and stored at –20°C were well preserved (p < 0.05); 2) sometimes, DNA was successfully extracted from samples stained with Rose Bengal. We recommend Guanidine lysis buffer with EDTA, stored at –20°C for up to six weeks, as the best protocol for preservation of DNA from porcelaneous foraminifera.

Publisher

GeoScienceWorld

Subject

Paleontology,Microbiology

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