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<journal-id journal-id-type="publisher">global-journal-of-science-frontier-research-c-biological-science</journal-id>
<journal-title-group>
<journal-title>Global Journal of Science Frontier Research - C: Biological Science</journal-title>
</journal-title-group>
<issn publication-format="print">0975-5896</issn>
<issn publication-format="electronic">2249-4626</issn>
<publisher><publisher-name>Global Journals Publishing Group Incorporated</publisher-name></publisher>
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<article-id pub-id-type="publisher-id">115697</article-id>
<title-group>
<article-title>Characterization of a Classical w14 Albino Mutation and a Putative New Robertsons Mutator-Induced Allele in Maize (Zea Mays)</article-title>
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<contrib-group>
<contrib contrib-type="author"><name><surname>Huynh</surname><given-names>Ngoc</given-names></name><xref ref-type="aff" rid="aff1" />
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<aff id="aff1">UNITED STATES, Midwestern State University</aff>
<pub-date publication-format="electronic" date-type="pub" iso-8601-date="2017-09-08">
<day>08</day>
<month>09</month>
<year>2017</year>
</pub-date>
<volume>17</volume>
<issue>C3</issue>
<abstract><p>The newly identified albino mutation, w*-5200, arose in a maize (Zea mays) population derived from Robertson’s Mutator transposon tagging crosses (Cook, 1988). Due to municipal water restrictions lasting three growing seasons, classical genetic allelism testing was not practical. Instead a molecular approach was pursued in an attempt to verify the genetic locus causing the mutant phenotype. Sequences of w*-5200 and 616B w14-N335 were compared to identify defects that would lead to inactivation of the gene in each, yielding evidence of neither a large-scale insertion nor any other obvious block to gene expression. Ultimately the lifting of water restrictions allowed a traditional allelism test, which verified that the novel mutation affects the w14 locus.</p></abstract>
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<p>The newly identified albino mutation, w*-5200, arose in a maize (Zea mays) population derived from Robertson’s Mutator transposon tagging crosses (Cook, 1988). Due to municipal water restrictions lasting three growing seasons, classical genetic allelism testing was not practical. Instead a molecular approach was pursued in an attempt to verify the genetic locus causing the mutant phenotype. Sequences of w*-5200 and 616B w14-N335 were compared to identify defects that would lead to inactivation of the gene in each, yielding evidence of neither a large-scale insertion nor any other obvious block to gene expression. Ultimately the lifting of water restrictions allowed a traditional allelism test, which verified that the novel mutation affects the w14 locus.</p>
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