Island Spider Halves DNA, Defying Evolutionary Norms | Quick Digest

Island Spider Halves DNA, Defying Evolutionary Norms | Quick Digest
A Canary Islands spider, *Dysdera tilosensis*, has surprisingly reduced its genome size by half, a phenomenon challenging established evolutionary theories for island species. This genetic streamlining occurred while paradoxically increasing its genetic diversity, leaving scientists intrigued by this unprecedented evolutionary path. The discovery forces a reevaluation of how species adapt to isolated environments.

Canary Islands spider, *Dysdera tilosensis*, cut genome by half.

Discovery challenges traditional island evolution theories.

Genome downsizing occurred without losing essential genes.

Despite smaller genome, spider shows higher genetic diversity.

Findings published in *Molecular Biology and Evolution*.

Scientists rethinking island colonization's genetic impact.

A groundbreaking scientific discovery from the Canary Islands has revealed that a unique spider species, *Dysdera tilosensis*, has undergone an extraordinary genetic transformation, reducing its genome size by nearly half over millions of years. This finding significantly challenges long-held evolutionary theories, particularly the 'founder effect,' which traditionally posits that species isolated on islands tend to accumulate repetitive, non-functional DNA and consequently expand their genomes while experiencing a drop in genetic diversity. Researchers, led by Julio Rozas and Sara Guirao from the University of Barcelona, found that *Dysdera tilosensis* now possesses approximately 1.7 billion DNA base pairs, a drastic reduction from its mainland relative, *Dysdera catalonica*, which has about 3.3 billion base pairs. What makes this case particularly puzzling for scientists is that despite this massive genetic streamlining, the island spider has simultaneously increased its genetic diversity, contrary to expectations. The spider achieved this 'genome downsizing' by shedding large stretches of repetitive and seemingly unnecessary DNA, often referred to as 'genomic junk,' without losing any genes critical for its survival. This efficient natural selection process, likely supported by stable and large island populations, allowed the removal of redundant genetic material, overturning assumptions about how isolation shapes evolution. The implications of this study, published in the journal *Molecular Biology and Evolution*, are global, prompting evolutionary biologists worldwide to reconsider the mechanisms of adaptation and genome evolution in isolated environments.
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