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Characterization of a complex satellite DNA in the mollusc Donax trunculus: Analysis of sequence variations and divergence
Institution:1. CAS Key Laboratory of Marine Ecology and Environmental Sciences, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China;2. Laboratory for Marine Ecology and Environmental Science, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266071, China;3. University of Chinese Academy of Sciences, Beijing 100049, China;1. Shanghai Engineering Research Center of Aquaculture and College of Fisheries and Life Science, Shanghai Ocean University, Shanghai 201306, China;2. Department of Fisheries and Allied Aquacultures, Auburn University, Auburn, AL 36849, USA;1. Norwegian University of Life Sciences, Faculty of Biosciences, PO Box 5003, 1432 Ås, Norway;2. Breeding and Genetics, AquaGen, PO Box 1240, 7462 Trondheim, Norway
Abstract:A highly repetitive sequence in the genomic DNA of the bivalve mollusc Donax trunculus (Dt) has been identified upon restriction with EcoRV. During the time-course of DNA digestion, genomic fragments resolved electrophoretically into a ladder-like banding pattern revealing a tandem arrangement of the repeated elements, thus representing satellite DNA sequences. Cloning and sequence analysis unraveled the presence of two groups of monomer units which can be considered distinctive satellite subfamilies. Each subclass is distinguishable by the presence of 17 evenly spread diagnostic nucleotides (nt). The respective consensus sequences are 155 bp in length and differ by 11%, while relevant internal substructures were not observed. The two satellite subfamilies constitute 0.23 and 0.09% of the Dt genome, corresponding to 20 000 and 7600 copies per haploid complement, respectively. Sequence mutations often appear to be shared between two or more monomer variants, indicating a high degree of homogenization as opposed to that of random mutational events. Shared mutations among variants appear either as single changes or in long stretches. This pattern may arise from gene conversion mechanisms acting at different levels, such as the spread of nt sequences of a similar length to the monomer repeat itself, and the diffusion of short tracts a few bp long. Subfamilies might have evolved from the occasional amplification and spreading of a monomer variant effected by gene conversion events
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