Genomic organization of the genes for human and mouse CC chemokine LEC

被引:15
作者
Fukuda, S
Hanano, Y
Iio, M
Miura, R
Yoshie, O
Nomiyama, H
机构
[1] Kumamoto Univ, Sch Med, Dept Biochem, Kumamoto 8600811, Japan
[2] Prefectural Univ Kumamoto, Fac Human Life Sci, Dept Food Sci & Nutr, Kumamoto 8628502, Japan
[3] Kinki Univ, Sch Med, Dept Bacteriol, Osaka 5898511, Japan
关键词
D O I
10.1089/104454999315330
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
Liver-expressed chemokine (LEC) is a CC chemokine that is selectively expressed in the liver. We report here the structures of the human and mouse genes for LEG. The human LEC gene (SCYA16) was isolated from a bacterial artificial chromosome (BAC) clone that also contained CC chemokine genes for MPIF-1/Ck beta 8, HCC-2/Lkn-1/MIP-5/MIP-1 delta, and HCC-1, The LEC gene is approximately 5.0 kb in length and has a three-exon and two-intron structure common to most CC chemokine genes. However, the promoter region is devoid of a typical TATA box, and transcription initiates at multiple sites. The gene for CC chemokine HCC-1, which is most similar to LEG, is located approximately 2.2 kb upstream from the 5' end of the LEC gene in a head-to-tail fashion. The mouse DNA fragment that hybridized with the human LEC cDNA was isolated from a BAC clone that also contained the CC chemokine genes for C10, MRP-2/CCF18/MIP-1 gamma, and RANTES, Sequence analysis revealed that the isolated gene does not encode a functional chemokine because of deletions, insertions, and base changes. Southern blot analysis revealed that the sequence isolated from the BAC clone was the only one hybridizing with human LEC cDNA in the mouse genome, Therefore, mice may have only an LEC pseudogene.
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页码:275 / 283
页数:9
相关论文
共 30 条
[1]   Human chemokines: An update [J].
Baggiolini, M ;
Dewald, B ;
Moser, B .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :675-705
[2]   THE GENE FOR C10, A MEMBER OF THE BETA-CHEMOKINE FAMILY, IS LOCATED ON MOUSE CHROMOSOME-11 AND CONTAINS A NOVEL 2ND EXON NOT FOUND IN OTHER CHEMOKINES [J].
BERGER, MS ;
KOZAK, CA ;
GABRIEL, A ;
PRYSTOWSKY, MB .
DNA AND CELL BIOLOGY, 1993, 12 (09) :839-847
[3]   Characterisation of macrophage inflammatory protein-5 human CC cytokine-2, a member of the macrophage-inflammatory-protein family of chemokines [J].
Coulin, F ;
Power, CA ;
Alouani, S ;
Peitsch, MC ;
Schroeder, JM ;
Moshizuki, M ;
ClarkLewis, I ;
Wells, TNC .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 248 (02) :507-515
[4]   LINE-1 - A MAMMALIAN TRANSPOSABLE ELEMENT [J].
FANNING, TG ;
SINGER, MF .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 910 (03) :203-212
[5]  
Farber JM, 1998, J INVEST MED, V46, P197
[6]   CK beta 8, a novel CC chemokine that predominantly acts on monocytes [J].
Forssmann, U ;
Delgado, MB ;
Uguccioni, M ;
Loetscher, P ;
Garotta, G ;
Baggiolini, M .
FEBS LETTERS, 1997, 408 (02) :211-216
[7]  
HARA T, 1995, J IMMUNOL, V155, P5352
[8]   Characterization of a novel CC chemokine, HCC-4, whose expression is increased by interleukin-10 [J].
Hedrick, JA ;
Helms, A ;
Vicari, A ;
Zlotnik, A .
BLOOD, 1998, 91 (11) :4242-4247
[9]   Databases on transcriptional regulation: TRANSFAC, TRRD and COMPEL [J].
Heinemeyer, T ;
Wingender, E ;
Reuter, I ;
Hermjakob, H ;
Kel, AE ;
Kel, OV ;
Ignatieva, EV ;
Ananko, EA ;
Podkolodnaya, OA ;
Kolpakov, FA ;
Podkolodny, NL ;
Kolchanov, NA .
NUCLEIC ACIDS RESEARCH, 1998, 26 (01) :362-367
[10]  
Lane D A, 1989, Baillieres Clin Haematol, V2, P961, DOI 10.1016/S0950-3536(89)80054-X