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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
The Immunoglobulin Heavy Chain Locus of the Duck
GENOMIC ORGANIZATION AND EXPRESSION OF D, J, AND C REGION
GENES*
Mats L.
Lundqvist ,
Darlene L.
Middleton ,
Starr
Hazard§, and
Gregory W.
Warr ¶
From the 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- - . No evidence for a functional
homologue (or remnant) of a gene was found. The 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 genes. The secreted forms of duck and µ are each
encoded by 4 constant region exons, and the hydrophobic C-terminal
regions of the membrane receptor forms of and µ are encoded by
one and two transmembrane exons, respectively. Putative switch (S)
regions were identified for duck µ and by comparison with chicken
Sµ and S sequences and for duck by comparison with mouse S .
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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