ANALYSIS OF THE GENOMIC SEQUENCE FOR THE AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (PKD1) GENE PREDICTS THE PRESENCE OF A LEUCINE-RICH REPEAT

被引:209
作者
BURN, TC
CONNORS, TD
DACKOWSKI, WR
PETRY, LR
VANRAAY, TJ
MILLHOLLAND, JM
VENET, M
MILLER, G
HAKIM, RM
LANDES, GM
KLINGER, KW
FENG, Q
ONUCHIC, LF
WATNICK, T
GERMINO, GG
DOGGETT, NA
机构
[1] VANDERBILT UNIV, MED CTR, DIV NEPHROL, NASHVILLE, TN 37232 USA
[2] JOHNS HOPKINS UNIV, SCH MED, DIV NEPHROL, BALTIMORE, MD 21205 USA
[3] LOS ALAMOS NATL LAB, DIV LIFE SCI, LOS ALAMOS, NM 87545 USA
[4] LOS ALAMOS NATL LAB, CTR HUMAN GENOME STUDIES, LOS ALAMOS, NM 87545 USA
关键词
D O I
10.1093/hmg/4.4.575
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
The complete genomic sequence of the gene responsible for the predominant form of polycystic kidney disease, PKD1, was determined to provide a framework for understanding the biology and evolution of the gene, and to aid in the development of molecular diagnostics. The DNA sequence of a 54 kb interval immediately upstream of the poly(A) addition signal sequence of the PKD1 transcript was determined, and then analyzed using computer methods. A leucine-rich repeat (LRR) motif was identified within the resulting predicted protein sequence of the PKD1 gene. By analogy with other LRR-containing proteins, this may explain some of the disease-related renal alterations such as mislocalization of membrane protein constituents and changes in the extracellular matrix organization. Finally, comparison of the genomic sequence and the published partial cDNA sequence showed several differences between the two sequences. The most significant difference detected predicts a novel carboxy-terminus for the PKD1 gene product.
引用
收藏
页码:575 / 582
页数:8
相关论文
共 70 条
[1]  
ADEMA GJ, 1994, J BIOL CHEM, V269, P20126
[2]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[3]   NUMBER OF CPG ISLANDS AND GENES IN HUMAN AND MOUSE [J].
ANTEQUERA, F ;
BIRD, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11995-11999
[4]   DIVERSITY IN G+C CONTENT AT THE 3RD POSITION OF CODONS IN VERTEBRATE GENES AND ITS CAUSE [J].
AOTA, S ;
IKEMURA, T .
NUCLEIC ACIDS RESEARCH, 1986, 14 (16) :6345-6355
[5]   THE SWISS-PROT PROTEIN-SEQUENCE DATA-BANK [J].
BAIROCH, A ;
BOECKMANN, B .
NUCLEIC ACIDS RESEARCH, 1992, 20 :2019-2022
[6]   FORMATION OF DNA TRIPLEXES ACCOUNTS FOR ARRESTS OF DNA-SYNTHESIS AT D(TC)N AND D(GA)N TRACTS [J].
BARAN, N ;
LAPIDOT, A ;
MANOR, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (02) :507-511
[7]   PHYSICAL CHARACTERISTICS IN EUKARYOTIC PROMOTERS [J].
BENSIMHON, M ;
GABARROARPA, J ;
EHRLICH, R ;
REISS, C .
NUCLEIC ACIDS RESEARCH, 1983, 11 (13) :4521-4540
[8]   INTRAMOLECULAR DNA TRIPLEXES, BENT DNA AND DNA UNWINDING ELEMENTS IN THE INITIATION REGION OF AN AMPLIFIED DIHYDROFOLATE-REDUCTASE REPLICON [J].
CADDLE, MS ;
LUSSIER, RH ;
HEINTZ, NH .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 211 (01) :19-33
[9]   AN UNUSUALLY LONG POLY(PURINE)-POLY(PYRIMIDINE) SEQUENCE IS LOCATED UPSTREAM FROM THE HUMAN THYROGLOBULIN GENE [J].
CHRISTOPHE, D ;
CABRER, B ;
BACOLLA, A ;
TARGOVNIK, H ;
POHL, V ;
VASSART, G .
NUCLEIC ACIDS RESEARCH, 1985, 13 (14) :5127-5144
[10]  
DANOVITCH GM, 1976, PERSPECTIVES NEPHROL, P125