Long-term conservation vs high sequence divergence: the case of an extraordinarily old satellite DNA in bivalve mollusks

• Published in: Heredity 2010-06, Vol.104 (6), p.543-551
• Main Authors: Plohl, M, Petrović, V, Luchetti, A, Ricci, A, Šatović, E, Passamonti, M, Mantovani, B
• Format: Article
• Language: English
• Subjects: Animals; Base Sequence; Biomedical and Life Sciences; Biomedicine; Bivalvia; Bivalvia - chemistry; Bivalvia - classification; Bivalvia - genetics; Cytogenetics; Deoxyribonucleic acid; DNA; DNA, Satellite; Donax trunculus; Ecology; Evolution, Molecular; Evolutionary Biology; Fluctuations; Genetic Variation; Genomics; Homogenization; Human Genetics; Molecular Sequence Data; Mollusks; original-article; Oysters; Phylogeny; Plant Genetics and Genomics; Pteriomorphia; Sequence Alignment
• ISSN: 0018-067X; 1365-2540
• DOI: 10.1038/hdy.2009.141

The ubiquity of satellite DNA (satDNA) sequences has raised much controversy over the abundance of divergent monomer variants and the long-time nucleotide sequence stability observed for many satDNA families. In this work, we describe the satDNA BIV160, characterized in nine species of the three main bivalve clades (Protobranchia, Pteriomorphia and Heteroconchia). BIV160 monomers are similar in repeat size and nucleotide sequence to satDNAs described earlier in oysters and in the clam Donax trunculus . The broad distribution of BIV160 satDNA indicates that similar variants existed in the ancestral bivalve species that lived about 540 million years ago; this makes BIV160 the most ancient satDNA described so far. In the species examined, monomer variants are distributed in quite a complex pattern. This pattern includes (i) species characterized by a specific group of variants, (ii) species that share distinct group(s) of variants and (iii) species with both specific and shared types. The evolutionary scenario suggested by these data reconciles sequence uniformity in homogenization-maintained satDNA arrays with the genomic richness of divergent monomer variants formed by diversification of the same ancestral satDNA sequence. Diversified repeats can continue to evolve in a non-concerted manner and behave as independent amplification-contraction units in the framework of a ‘library of satDNA variants’ representing a permanent source of monomers that can be amplified into novel homogeneous satDNA arrays. On the whole, diversification of satDNA monomers and copy number fluctuations provide a highly dynamic genomic environment able to form and displace satDNA sequence variants rapidly in evolution.