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Vol. 10, Issue 8, 1095-1102, August 2000
REPORT
Genomic Sequence Analysis of the Mouse Naip Gene Array
Matthew G.
Endrizzi,2,4
Vey
Hadinoto,2
Joseph D.
Growney,2
Webb
Miller,3 and
William F.
Dietrich1,2,5
1 Howard Hughes Medical Institute and 2 Department
of Genetics, Harvard Medical School, Boston, Massachusetts 02115 USA;
3 Department of Computer Science and Engineering, Pennsylvania
State University, University Park, Pennsylvania 16802 USA
A mouse locus called Lgn1 determines differences in
macrophage permissiveness for the intracellular replication of
Legionella pneumophila. The only regional candidate genes for
this phenotype difference lie within a cluster of closely linked
paralogs of the Neuronal Apoptosis Inhibitory Protein (Naip)
gene. Previous genetic and physical mapping of the Lgn1
phenotype narrowed it to an interval containing only Naip2
and Naip5, suggesting that there is not complete
functional overlap among the mouse Naip loci. In order to
gather more information about polymorphisms among the Naip
genes of the 129 mouse haplotype, we have determined the genomic
sequence of a substantial portion of the 129 Naip gene array.
We have constructed an evolutionary model for the expansion of the
Naip gene array from a single progenitor Naip gene.
This model predicts the presence of two distinct families of
Naip paralogs: Naip1/2/3 and Naip4/5/6/7.
Unlike the divergences among all the other Naip paralogs, the
splits among Naip4, Naip5, Naip6, and
Naip7 occurred relatively recently. The high degree of
sequence conservation within the Naip4/5/6/7 family increases the likelihood of functional overlap among these genes.
[The
sequence data described in this paper have been submitted to the
GenBank data library under accession nos. AF242431-AF242435.]
4
Present address: Whitehead Institute/MIT Center for
Genome Research, Cambridge, MA 02142.
5
Corresponding author.
10:1095-1102 ©2000 by Cold Spring Harbor Laboratory Press ISSN 1088-9051/00 $5.00

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