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   <ui>gb-spotlight-20020422-02</ui>
   <ji>GBJ</ji>
   <fm>
      <dochead>Research news</dochead>
      <bibl>
         <title>
            <p>FOXO transcription factor stimulates repair</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Weitzman</snm>
               <mi>B</mi>
               <fnm>Jonathan</fnm>
               <email>jonathanweitzman@hotmail.com</email>
            </au>
         </aug>
         <source>Genome Biology</source>
         <issn>1465-6906</issn>
         <pubdate>2002</pubdate>
         <volume>3</volume>
         <fpage>spotlight-20020422-02</fpage>
         <xrefbib>
            <pubid idtype="doi">10.1186/gb-spotlight-20020422-02</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>22</day>
               <month>4</month>
               <year>2002</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2002</year>
         <collab>BioMed Central Ltd</collab>
      </cpyrt>
      <shortabs>
         <p>A member of the FOXO family of forkhead transcription factors regulates cell-cycle and DNA repair pathways under stress.</p>
      </shortabs>
   </fm>
   <meta>
      <classifications>
         <classification type="news" subtype="status">Archive</classification>
      </classifications>
   </meta>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p>The protein kinase <abbr bid="B1">Akt</abbr> promotes cell survival by phosphorylating and inhibiting FOXO forkhead transcription factors. FOXO factors have been linked to stress responses and the regulation of longevity. In the April 19 <abbr bid="B2"><it>Science</it></abbr>, Hien Tran and colleagues at <abbr bid="B3">Boston's Children's Hospital</abbr> define a role for the <abbr bid="B4">FOXO3a</abbr> family member in the response to DNA damage (<it>Science</it> 2002, <b>296</b>:530-534). They created a Rat-1 fibroblast cell line expressing a tamoxifen-inducible FOXO3a protein. FOXO3a expression resulted in a delay in G2-M phase of the cell-cycle and enhanced DNA repair. Tran <it>et al.</it> performed a microarray screen to find FOXO3a-regulated genes and identified a number of genes involved in apoptosis and cell cycle regulation. They report that FOXO3a directly regulates transcription of the <it>GADD45A</it> gene upon damage of cellular DNA, and the ability of FOXO3a to induce DNA repair was reduced in cells lacking GADD45A. The role of FOXO3a in DNA repair, cell-cycle regulation and apoptosis probably contributes to its effect on organism life span.</p>
      </sec>
   </bdy>
   <bm>
      <refgrp>
         <bibl id="B1">
            <note>Akt promotes cell survival by phosphorylating and inhibiting a Forkhead transcription factor.</note>
            <xrefbib>
               <pubid idtype="pmpid" link="fulltext">10102273</pubid>
            </xrefbib>
         </bibl>
         <bibl id="B2">
            <url>http://www.sciencemag.org/</url>
            <note>
               <it>Science</it>
            </note>
         </bibl>
         <bibl id="B3">
            <url>http://www.tch.harvard.edu</url>
            <note>Children's Hospital Boston</note>
         </bibl>
         <bibl id="B4">
            <note>AFX-like Forkhead transcription factors mediate cell-cycle regulation by Ras and PKB through p27kip1.</note>
            <xrefbib>
               <pubid idtype="pmpid" link="fulltext">10783894</pubid>
            </xrefbib>
         </bibl>
      </refgrp>
   </bm>
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