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<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>10</Volume>
				<Issue>2</Issue>
				<PubDate PubStatus="epublish">
					<Year>1999</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>CLONING AND EXPRESSION OF A HUMAN
INTERFERON a2 GENE IN E. COLI</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31487</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		    <Abstract>The plasmid pALCA1SIFN containing cDNA that encodes the human interferon
a-2b was obtained from the ATCC(no. 531667). In this system the expression of the
gene is under the control of an alcA promoter. alcA p is a specific promoter for
expression of different genes in Aspergillusfilamentous. In this plasmid the coding
region of IFN?-2b is preceded by the coding region of a synthetic signal peptide. For
direct expression of the IFNa-2b gene under the control of a T7/lac promotor of
pET24d(+) expression vector, three subcloning steps were carried out which resulted
in the construction of 3 new plamids. pHA1, pHA2 and pHA4 in which the IFNa-2
gene is under the control of lacp, lacuv5p and T7 promoter, respectively. Another
plasrnid, pHA3, was also constiucted and is a modified version of pET24d(+).
Provided there is a synthetic signal peptide preceding the coding region of IFNa2
gene, the protein can be seen in either system, as shown by western blotting, albeit
with a different level of expression. The best product can be seen in the pHA4plasmid
with a T7 pas judged by dot and western blotting</Abstract>
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