Characterization of TH1 and CTSZ, two non-imprinted genes downstream of GNAS1 in chromosome 20q13

被引:22
作者
Bonthron, DT
Hayward, BE
Moran, V
Strain, L
机构
[1] Univ Leeds, St Jamess Univ Hosp, Mol Med Unit, Leeds LS9 7TF, W Yorkshire, England
[2] Univ Edinburgh, Western Gen Hosp, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
基金
英国惠康基金;
关键词
D O I
10.1007/s004390000344
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The clustering and coordinate regulation of many imprinted genes justifies positional searches for imprinted genes adjacent to known ones. We recently characterized a locus on 20q13, containing GNAS1, which has a highly complex imprinted expression pattern. In a search for neighbouring genes, we have now characterized a new gene, TH1, downstream of GNAS1. TH1 and GNAS1 are separated by more than 70 kb consisting largely of interspersed repetitive DNA, TH1 is the homologue of a gene that, in Drosophila, lies adjacent to the DNA repair gene mei-41. We have determined the full-length structures of human, mouse and Drosophila TH1. Though of unknown function, TH1 is highly conserved and widely expressed. Nonetheless, there is no similar Caenorhabditis elegans protein. We have also determined the complete genomic structures of human and Drosophila TH1. The Drosophila gene has five exons spanning 2.6 kb. The last three introns have precise equivalents in the human gene, which has 15 exons spanning 14 kb and is transcribed away from GNAS1. Using a single-nucleotide polymorphism in the 3' untranslated region, we have demonstrated biallelic TH1 expression in human fetal tissues, suggesting that, unlike GNAS1, TH1 is probably not imprinted. Immediately downstream of TH1 lies CTSZ, encoding the recently described cysteine protease, cathepsin Z. We have also elucidated the genomic structure of this gene; it has sis exons spanning 12 kb and is oriented tail-to-tail with TH1, only 70 bp separating their polyadenylation sites. A polymorphism was again identified within the CTSZ 3' untranslated legion and used to demonstrate biallelic expression in fetal tissues.
引用
收藏
页码:165 / 175
页数:11
相关论文
共 25 条
  • [11] An imprinted antisense transcript at the human GNAS1 locus
    Hayward, BE
    Bonthron, DT
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (05) : 835 - 841
  • [12] Bidirectional imprinting of a single gene:: GNAS1 encodes maternally, paternally, and biallelically derived proteins
    Hayward, BE
    Moran, V
    Strain, L
    Bonthron, DT
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) : 15475 - 15480
  • [13] The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins
    Hayward, BE
    Kamiya, M
    Strain, L
    Moran, V
    Campbell, R
    Hayashizaki, Y
    Bonthron, DT
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) : 10038 - 10043
  • [14] Ischia R, 1997, J BIOL CHEM, V272, P11657
  • [15] The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region
    Jay, P
    Rougeulle, C
    Massacrier, A
    Moncla, A
    Mattei, MG
    Malzac, P
    Roeckel, N
    Taviaux, S
    Lefranc, JLB
    Cau, P
    Berta, P
    Lalande, M
    Muscatelli, F
    [J]. NATURE GENETICS, 1997, 17 (03) : 357 - 361
  • [16] A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region
    Jong, MTC
    Gray, TA
    Ji, YG
    Glenn, CC
    Saitoh, S
    Driscoll, DJ
    Nicholls, RD
    [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (05) : 783 - 793
  • [17] KEHLENBACH RH, 1994, NATURE, V372, P804
  • [18] Human cathepsin X:: A novel cysteine protease of the papain family with a very short proregion and unique insertions
    Nägler, DK
    Ménard, R
    [J]. FEBS LETTERS, 1998, 434 (1-2) : 135 - 139
  • [19] Human cathepsin X:: A cysteine protease with unique carboxypeptidase activity
    Nägler, DK
    Zhang, RL
    Tam, W
    Sulea, T
    Purisima, EO
    Ménard, R
    [J]. BIOCHEMISTRY, 1999, 38 (39) : 12648 - 12654
  • [20] Imprinting in Prader-Willi and Angelman syndromes
    Nicholls, RD
    Saitoh, S
    Horsthemke, B
    [J]. TRENDS IN GENETICS, 1998, 14 (05) : 194 - 200