<?xml version='1.0' encoding='utf-8'?>
<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:contributor>Zhenfang Xia</dc:contributor>
  <dc:contributor>William L. Gale</dc:contributor>
  <dc:contributor>Chunfa Wu</dc:contributor>
  <dc:contributor>Alec G. Maule</dc:contributor>
  <dc:contributor>Xiaotian Chang</dc:contributor>
  <dc:creator>Reynaldo Patino</dc:creator>
  <dc:date>2000</dc:date>
  <dc:description>&lt;p&gt;Complementary DNA libraries from liver and ovary of an immature female channel catfish were screened with a homologous ER&amp;alpha; cDNA probe. The hepatic library yielded two new channel catfish ER cDNAs that encode N-terminal ER&amp;alpha; variants of different sizes. Relative to the catfish ER&amp;alpha; (medium size; 581 residues) previously reported, these new cDNAs encode Long-ER&amp;alpha; (36 residues longer) and Short-ER&amp;alpha; (389 residues shorter). The 5&amp;prime;-end of Long-ER&amp;alpha; cDNA is identical to that of Medium-ER&amp;alpha; but has an additional 503-bp segment with an upstream, in-frame translation-start codon. Recombinant Long-ER&amp;alpha; binds estrogen with high affinity (&lt;i&gt;K&lt;/i&gt;&lt;sub&gt;d&lt;/sub&gt; = 3.4 nM), similar to that previously reported for Medium-ER&amp;alpha; but lower than reported for catfish ER&amp;beta;. Short-ER&amp;alpha; cDNA encodes a protein that lacks most of the receptor protein and does not bind estrogen. Northern hybridization confirmed the existence of multiple hepatic ER&amp;alpha; RNAs that include the size range of the ER&amp;alpha; cDNAs obtained from the libraries as well as additional sizes. Using primers for RT-PCR that target locations internal to the protein-coding sequence, we also established the presence of several ER&amp;alpha; cDNA variants with in-frame insertions in the ligand-binding and DNA-binding domains and in-frame or out-of-frame deletions in the ligand-binding domain. These internal variants showed patterns of expression that differed between the ovary and liver. Further, the ovarian library yielded a full-length, ER&amp;alpha; antisense cDNA containing a poly(A) signal and tail. A limited survey of histological preparations from juvenile catfish by &lt;i&gt;in situ&lt;/i&gt; hybridization using directionally synthesized cRNA probes also suggested the expression of ER&amp;alpha; antisense RNA in a tissue-specific manner. In conclusion, channel catfish seemingly have three broad classes of ER&amp;alpha; mRNA variants: those encoding N-terminal truncated variants, those encoding internal variants (including C-terminal truncated variants), and antisense mRNA. The sense variants may encode functional ER&amp;alpha; or related proteins that modulate ER&amp;alpha; or ER&amp;beta; activity. The existence of ER antisense mRNA is reported in this study for the first time. Its role may be to participate in the regulation of ER gene expression.&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1006/gcen.2000.7566</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Elsevier</dc:publisher>
  <dc:title>Novel transcripts of the estrogen receptor α  gene in channel catfish</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>