Homologues to the first gene for autosomal dominant polycystic kidney disease are pseudogenes

被引:68
作者
Bogdanova, N
Markoff, A
Gerke, V
McCluskey, M
Horst, J
Dworniczak, B
机构
[1] WWU Munster, Inst Humangenet, D-48149 Munster, Germany
[2] WWU Munster, ZMBE, Inst Med Biochem, D-48149 Munster, Germany
[3] Edith Cowan Univ, Ctr Human Genet, Jondaloop, Australia
关键词
D O I
10.1006/geno.2001.6568
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
PKD1 is the first gene identified to be causative for the condition of autosomal dominant polycystic kidney disease. There are several genes homologous to PKD1 that are located proximal to the master gene on the same chromosome. Two of these genes have been recently covered in a large sequencing work on chromosome 16, and their structure has been broadly analyzed. However, the major question whether homologous genes (HG) code for functionally active polypeptides has not been resolved so far. The current study identifies and partially characterizes four more homologues of PKD1, different from the previously published sequence, two of which were found by screening of a BAC library and the other two contained in available databases. Analysis of HG transcripts shows that they are not translated in the model cell line T98G. Taken together, these findings suggest that homologues to PKD1 form a family of pseudogenes. (C) 2001 Academic Press.
引用
收藏
页码:333 / 341
页数:9
相关论文
共 27 条
  • [1] BOGDANOVA N, 1995, HUM GENET, V95, P645
  • [2] RNAs from all categories generate retrosequences that may be exapted as novel genes or regulatory elements
    Brosius, J
    [J]. GENE, 1999, 238 (01) : 115 - 134
  • [3] ANALYSIS OF THE GENOMIC SEQUENCE FOR THE AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (PKD1) GENE PREDICTS THE PRESENCE OF A LEUCINE-RICH REPEAT
    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
    [J]. HUMAN MOLECULAR GENETICS, 1995, 4 (04) : 575 - 582
  • [4] Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
    Cavaillé, J
    Buiting, K
    Kiefmann, M
    Lalande, M
    Brannan, CI
    Horsthemke, B
    Bachellerie, JP
    Brosius, J
    Hüttenhofer, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) : 14311 - 14316
  • [5] DALGAARD O Z, 1957, Acta Med Scand Suppl, V328, P1
  • [6] EVIDENCE FOR A 3RD GENETIC-LOCUS FOR AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE
    DAOUST, MC
    REYNOLDS, DM
    BICHET, DG
    SOMLO, S
    [J]. GENOMICS, 1995, 25 (03) : 733 - 736
  • [7] AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE - EVIDENCE FOR THE EXISTENCE OF A 3RD LOCUS IN A PORTUGUESE FAMILY
    DEALMEIDA, S
    DEALMEIDA, E
    PETERS, D
    PINTO, JR
    TAVORA, I
    LAVINHA, J
    BREUNING, M
    PRATA, MM
    [J]. HUMAN GENETICS, 1995, 96 (01) : 83 - 88
  • [8] GLUCKSMANNKUIS MA, 1995, CELL, V81, P289
  • [9] Co-assembly of polycystin-1 and-2 produces unique cation-permeable currents
    Hanaoka, K
    Qian, F
    Boletta, A
    Bhumia, AK
    Piontek, K
    Tsiokas, L
    Sukhatme, VP
    Guggino, WB
    Germino, GG
    [J]. NATURE, 2000, 408 (6815) : 990 - 994
  • [10] THE POLYCYSTIC KIDNEY-DISEASE-1 (PKD1) GENE ENCODES A NOVEL PROTEIN WITH MULTIPLE CELL RECOGNITION DOMAINS
    HUGHES, J
    WARD, CJ
    PERAL, B
    ASPINWALL, R
    CLARK, K
    SANMILLAN, JL
    GAMBLE, V
    HARRIS, PC
    [J]. NATURE GENETICS, 1995, 10 (02) : 151 - 160