Genomic sequence analysis of the mouse Naip gene array

被引:52
作者
Endrizzi, MG
Hadinoto, V
Growney, JD
Miller, W
Dietrich, WF [1 ]
机构
[1] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[3] Penn State Univ, Dept Comp Sci & Engn, University Pk, PA 16802 USA
关键词
D O I
10.1101/gr.10.8.1095
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1095 / 1102
页数:8
相关论文
共 33 条
[1]  
Ansari-Lari MA, 1998, GENOME RES, V8, P29
[2]   NATURAL-RESISTANCE TO INFECTION WITH LEGIONELLA-PNEUMOPHILA - CHROMOSOMAL LOCALIZATION OF THE LGN1 SUSCEPTIBILITY GENE [J].
BECKERS, MC ;
YOSHIDA, S ;
MORGAN, K ;
SKAMENE, E ;
GROS, P .
MAMMALIAN GENOME, 1995, 6 (08) :540-545
[3]   Prediction of complete gene structures in human genomic DNA [J].
Burge, C ;
Karlin, S .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 268 (01) :78-94
[4]   ORDERED SHOTGUN SEQUENCING, A STRATEGY FOR INTEGRATED MAPPING AND SEQUENCING OF YAC CLONES [J].
CHEN, EY ;
SCHLESSINGER, D ;
KERE, J .
GENOMICS, 1993, 17 (03) :651-656
[5]   EFFECTIVE AMPLIFICATION OF LONG TARGETS FROM CLONED INSERTS AND HUMAN GENOMIC DNA [J].
CHENG, S ;
FOCKLER, C ;
BARNES, WM ;
HIGUCHI, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (12) :5695-5699
[6]   LGN1, A GENE THAT DETERMINES SUSCEPTIBILITY TO LEGIONELLA-PNEUMOPHILA, MAPS TO MOUSE CHROMOSOME-13 [J].
DIETRICH, WF ;
DAMRON, DM ;
ISBERG, RR ;
LANDER, ES ;
SWANSON, MS .
GENOMICS, 1995, 26 (03) :443-450
[7]   Genetic and physical mapping of the mouse host resistance locus Lgn1 [J].
Diez, E ;
Beckers, MC ;
Ernst, E ;
DiDonato, CJ ;
Simard, LR ;
Morissette, C ;
Gervais, F ;
Yoshida, SI ;
Gros, P .
MAMMALIAN GENOME, 1997, 8 (09) :682-685
[8]   The neuronal apoptosis inhibitory protein (Naip) is expressed in macrophages and is modulated after phagocytosis and during intracellular infection with Legionella pneumophila [J].
Diez, E ;
Yaraghi, Z ;
MacKenzie, A ;
Gros, P .
JOURNAL OF IMMUNOLOGY, 2000, 164 (03) :1470-1477
[9]   Comparative sequence analysis of the mouse and human Lgn1/SMA interval [J].
Endrizzi, M ;
Huang, S ;
Scharf, JM ;
Kelter, AR ;
Wirth, B ;
Kunkel, LM ;
Miller, W ;
Dietrich, WF .
GENOMICS, 1999, 60 (02) :137-151
[10]   MOLECULAR-CLONING AND CHARACTERIZATION OF THE HUMAN BETA-LIKE GLOBIN GENE-CLUSTER [J].
FRITSCH, EF ;
LAWN, RM ;
MANIATIS, T .
CELL, 1980, 19 (04) :959-972