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Vol. 10, Issue 3, 302-310, March 2000
LETTER
Evolution of the Neuropeptide Y Receptor Family: Gene and Chromosome Duplications Deduced from the Cloning and Mapping of the Five Receptor Subtype Genes in Pig
Amanda
Wraith,1
Anna
Törnsten,2
Patrick
Chardon,3
Ingrid
Harbitz,4
Bhanu P.
Chowdhary,5
Leif
Andersson,2
Lars-Gustav
Lundin,6 and
Dan
Larhammar1,7
1 Department of Neuroscience, Unit of Pharmacology, Uppsala
University, SE-751 24 Uppsala, Sweden; 2 Department of Animal
Breeding and Genetics, Swedish University of Agricultural Sciences,
SE-751 24 Uppsala, Sweden; 3 Laboratoire de Radiobiologie
Appliquée, CEA-INRA, Jouy en Josas 78350, France;
4 Department of Biochemistry, Physiology and Nutrition, The
Norwegian School of Veterinary Science, N-0033 Oslo, Norway;
5 Division of Animal Genetics, The Royal Veterinary & Agricultural University, 1870 Frederiksberg, Denmark;
6 Department of Medical Biochemistry and Microbiology, Uppsala
University, SE-751 23 Uppsala, Sweden
Neuropeptide Y (NPY) receptors mediate a variety of physiological
responses including feeding and vasoconstriction. To investigate the
evolutionary events that have generated this receptor family, we have
sequenced and determined the chromosomal localizations of all five
presently known mammalian NPY receptor subtype genes in the domestic
pig, Sus scrofa (SSC). The orthologs of the Y1 and
Y2 subtypes display high amino acid sequence identities
between pig, human, and mouse (92%-94%), whereas the Y4,
Y5, and y6 subtypes display lower identities
(76%-87%). The lower identity of Y5 is due to high
sequence divergence in the large third intracellular loop. The
NPY1R, NPY2R, and NPY5R receptor genes were
localized to SSC8, the NPY4R to SSC14, and
NPY6R to SSC2. Our comparisons strongly suggest that the tight
cluster of NPY1R, NPY2R, and NPY5R on human
chromosome 4 (HSA4) represents the ancestral configuration, whereas the
porcine cluster has been split by two inversions on SSC8. These 3 genes, along with adjacent genes from 14 other gene families, form a
cluster on HSA4 with extensive similarities to a cluster on HSA5, where
NPY6R and >13 other paralogs reside, as well as another
large cluster on HSA10 that includes NPY4R. Thus, these gene
families have expanded through large-scale duplications. The sequence
comparisons show that the NPY receptor triplet
NPY1R-NPY2R-NPY5R existed before these
large-scale duplications.
[Sequence data for this article
were deposited with the GenBank data library under accession nos.
AF106081, PID g6457648 (for Pig Y1 sequence); accession nos. AF106082,
PID g4249727 (for Pig Y2 sequence); accession no. AF227955 (for Pig Y4
sequence); accession nos. AF106083, PID g4249729 (for Pig Y5 sequence); accession no. AF227956 (for Pig Y6 sequence).]
7
Corresponding author.
10:302-310 ©2000 by Cold Spring Harbor Laboratory Press ISSN 1088-9051/00 $5.00

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