<?xml version="1.0"?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-16T03:06:01Z</responseDate><request verb="GetRecord" metadataPrefix="oai_dc">https://repository.lib.bcit.ca/oai/request</request><GetRecord><record><header><identifier>oai:repository.lib.bcit.ca:node-1713</identifier><datestamp>2025-05-12T18:14:50Z</datestamp><setSpec>node:32</setSpec><setSpec>oai_pmh:all_repository_items</setSpec></header><metadata><oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>In silico evolution of the hunchback gene indicates redundancy in cis-regulatory organization and spatial gene expression</dc:title>
                  <dc:description>Biological development depends on the coordinated expression of genes in time and space. Developmental genes have extensive cis-regulatory regions which control their expression. These regions are organized in a modular manner, with different modules controlling expression at different times and locations. Both how modularity evolved and what function it serves are open questions. We present a computational model for the cis-regulation of the hunchback (hb) gene in the fruit fly (Drosophila). We simulate evolution (using an evolutionary computation approach from computer science) to find the optimal cis-regulatory arrangements for fitting experimental hb expression patterns. We find that the cis-regulatory region tends to readily evolve modularity. These cis-regulatory modules (CRMs) do not tend to control single spatial domains, but show a multi-CRM/multi-domain correspondence. We find that the CRM-domain correspondence seen in Drosophila evolves with a high probability in our model, supporting the biological relevance of the approach. The partial redundancy resulting from multi-CRM control may confer some biological robustness against corruption of regulatory sequences. The technique developed on hb could readily be applied to other multi-CRM developmental genes.,Peer reviewed,Published.</dc:description>
                  <dc:date>2014-04</dc:date>
                  <dc:identifier>doi: 10.1142/S0219720014410091</dc:identifier>
          <dc:identifier>accessnum: NIHMS583031</dc:identifier>
          <dc:identifier>pmc: PMC4068237</dc:identifier>
                  <dc:language>English</dc:language>
                  <dc:contributor>Holloway, David</dc:contributor>
          <dc:contributor>Zagrijchuk, Elizaveta A.</dc:contributor>
          <dc:contributor>Sabirov, Marat A.</dc:contributor>
          <dc:contributor>Spirov, Alexander V.</dc:contributor>
                  <dc:publisher>Imperial College Press</dc:publisher>
                  <dc:type>Text</dc:type>
                  <dc:rights>© 2014 Imperial College Press</dc:rights></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>
