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  <front>

    <journal-meta>

      <journal-title>Pakistan Journal of Biological Sciences</journal-title>

      <issn pub-type="ppub">1028-8880</issn>

      <issn pub-type="epub">1812-5735</issn>

      <publisher>

        <publisher-name>Asian Network for Scientific Information</publisher-name>

      </publisher>

    </journal-meta>


    <article-meta>

      <article-id pub-id-type="doi">10.3923/pjbs.2009.101.109</article-id>


      <title-group>

        <article-title><![CDATA[Genetic Transformation of Nepalese Spring Wheat (<I>Triticum aestivum 
        </I>L.) Cultivars with<I> ipt </I>Gene under the Regulation of a Senescence 
        Enhanced Promoter from Maize]]></article-title>

      </title-group>


      <contrib-group>

        <contrib contrib-type="author" xlink:type="simple">


          <name name-style="western">

            <surname>Pant</surname>

            <given-names>D.R.</given-names>

          </name>


          <name name-style="western">

            <surname>Bhattarai</surname>

            <given-names>T.</given-names>

          </name>


          <name name-style="western">

            <surname>Beck</surname>

            <given-names>E.</given-names>

          </name>


          <name name-style="western">

            <surname>Fettig</surname>

            <given-names>S.</given-names>

          </name>


        </contrib>

      </contrib-group>


      <pub-date pub-type="collection">


        <month>2</month>




        <year>2009</year>

      </pub-date>


      <volume>12</volume>

      <issue>2</issue>


      <abstract><![CDATA[<p>Two Nepalese spring wheat cultivars were transformed 
        with an<I> ipt </I>gene from <I>Agrobacterium</I> <I>tumefaciens</I> under 
        the control of the senescence inducible promoter pSEE1 from maize using 
        biolistic method. The resulting transgenic lines, one from Pasang Lahmu 
        and seven from Annapurna-1, were studied for the expression of the transgene 
        and the phenotype characters like chlorophyll content, chlorophylla/b 
        ratio, PS II quantum yield and other parameters of agronomic importance. 
        Analysis of transgene expression by RT-PCR revealed very weak or no signal 
        at all, indicating either partial or complete silencing of the transgene 
        in the lines tested. None of the plants exhibited a phenotype that was 
        significantly different from the respective azygous controls.</p>]]></abstract>


    </article-meta>

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