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<p>to genomic instability and a variety of carcinomas.</p>

<p><big> History and structure </big></p>
<p>The minichromosome maintenance proteins were named after a yeast genetics screen for mutants defective in the regulation of DNA replication initiation.  The rationale behind this screen was that if replication origins were regulated in a manner analogous to transcription promoters, where transcriptional regulators showed promoter specificity, then replication regulators should also show origin specificity.  Since eukaryotic chromosomes contain multiple</p><p>
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