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Originally published In Press as doi:10.1074/jbc.M106221200 on October 9, 2001

J. Biol. Chem., Vol. 276, Issue 50, 46729-46736, December 14, 2001
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The Immunoglobulin Heavy Chain Locus of the Duck
GENOMIC ORGANIZATION AND EXPRESSION OF D, J, AND C REGION GENES*

Mats L. LundqvistDagger , Darlene L. MiddletonDagger , Starr Hazard§, and Gregory W. WarrDagger

From the Dagger  Department of Biochemistry and Molecular Biology and § Biomolecular Computing Resource, Medical University of South Carolina, Charleston, South Carolina 29425

The region of the duck IgH locus extending from upstream of the proximal diversity (D) segment to downstream of the constant gene cluster has been cloned and mapped. A sequence contig of 48,796 base pairs established that the organization of the genes is D-JH-µ-alpha -upsilon . No evidence for a functional homologue (or remnant) of a delta  gene was found. The alpha  gene is in inverted transcriptional orientation; class switch to IgA expression thus requires inversion of the ~27-kilobase pair region that includes both µ and alpha  genes. The secreted forms of duck alpha  and µ are each encoded by 4 constant region exons, and the hydrophobic C-terminal regions of the membrane receptor forms of alpha  and µ are encoded by one and two transmembrane exons, respectively. Putative switch (S) regions were identified for duck µ and upsilon  by comparison with chicken Sµ and Supsilon sequences and for duck alpha  by comparison with mouse Salpha . The duck IgH locus is rich in complex variable number tandem repeats, which occupy ~60% of the sequenced region, and occur at a much higher frequency in the IgH locus than in other sequenced regions of the duck genome.


* This work was supported by National Institutes of Health Grant RO1AI45111, the United States Department of Agriculture Grant NRICGP 96352053663, and by the Medical University of South Carolina.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the DDBJ/GenBankTM/EBI Data Bank with accession number(s) AJ314750, AJ314751, AJ314752, AJ314753, AJ314754, AJ314755, and AJ314756.

To whom correspondence should be addressed: Dept. of Biochemistry and Molecular Biology, Medical University of South Carolina, 173 Ashley Ave., P. O. Box 250509, Charleston, SC 29425. Tel.: 843-792-0597; Fax: 843-792-4850; E-mail: warrgw@musc.edu.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.
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