Fiber-FISH analysis of the 3′-terminal region of the human L-type Ca2+ channel α1C subunit gene

被引:5
|
作者
Liu, WS
Soldatov, NM
Gustavsson, I
Chowdhary, BP
机构
[1] Swedish Univ Agr Sci, Dept Anim Breeding & Genet, Uppsala, Sweden
[2] Georgetown Univ, Med Ctr, Dept Pharmacol, Washington, DC 20001 USA
关键词
D O I
10.1111/j.1601-5223.1998.00169.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Human L-type Ca2+ channel alpha(1C) subunit gene (CACNLlAl) maps to the distal region of chromosome 12p13, and is composed of approximate to 50 exons spanning over 150 kb of the human genome as estimated by restriction map analysis. However, the structure and the total length of the 3'-end of the gene is not clear because the size of several big introns remains unknown. Here the fiber-FISH technique was used to determine the relative order and size of eight partial genomic DNA clones from the central and 3'-terminal regions of CACNlAl. The total physical distance of this region, including the size and gap distances between the clones were re-estimated. The results show that the physical order of the tested clones was 5'- g14-5 > g12-2 > g10-8 > g4-5 > g16-7 > g8-3 > g12-5 > g6-20 -3'. Their individual sizes Vary between 6.7 and 21.9 kb. Clones g6-20 and g12-5, both containing repetitive exon 45/46-like element; were found to be located within 59.1 kb downstream of g8-3 containing earlier identified polyadenylation site, i.e. 229.5 kb away from clone g14-5 (exons 10, 11). The possible implications of this structural complexity is discussed.
引用
收藏
页码:169 / 175
页数:7
相关论文
共 50 条
  • [1] Role of carboxyl terminal region of L-type Ca2+ channel α1C subunit (Cav1.2) in the Ca2+ channel inactivation.
    Komuro, Y
    Nagao, T
    Ichijo, H
    Adachi-Akahane, S
    JOURNAL OF PHARMACOLOGICAL SCIENCES, 2003, 91 : 243P - 243P
  • [2] Farnesol blocks the L-type Ca2+ channel by targeting the α1C subunit
    Luft, UC
    Bychkov, R
    Gollasch, M
    Gross, V
    Roullet, JB
    McCarron, DA
    Ried, C
    Hofmann, F
    Yagil, Y
    Yagil, C
    Haller, H
    Luft, FC
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (04) : 959 - 966
  • [3] Clotrimazole inhibits the recombinant human cardiac L-type Ca2+ channel α1C subunit
    Fearon, IM
    Ball, SG
    Peers, C
    BRITISH JOURNAL OF PHARMACOLOGY, 2000, 129 (03) : 547 - 554
  • [4] Hypoxia inhibits the recombinant alpha(1C) subunit of the human cardiac L-type Ca2+ channel
    Fearon, IM
    Palmer, ACV
    Balmforth, AJ
    Ball, SG
    Mikala, G
    Schwartz, A
    Peers, C
    JOURNAL OF PHYSIOLOGY-LONDON, 1997, 500 (03): : 551 - 556
  • [5] L-type Ca2+ channel α1c subunit isoform switching in failing human ventricular myocardium
    Yang, YB
    Chen, XW
    Margulies, K
    Jeevanandam, V
    Pollack, P
    Bailey, BA
    Houser, SR
    JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2000, 32 (06) : 973 - 984
  • [6] Analysis of oxygen-sensitive human cardiac L-type Ca2+ channel α1C subunit (hHT isoform)
    Scragg, JL
    Fearon, IM
    Ball, SG
    Schwartz, A
    Varadi, G
    Peers, C
    OXYGEN SENSING, 2004, 381 : 290 - 302
  • [7] New Molecular Determinant for Inactivation of the Human L-Type α1C Ca2+ Channel
    N.M. Soldatov
    S. Zhenochin
    B. AlBanna
    D.R. Abernethy
    M. Morad
    The Journal of Membrane Biology, 2000, 177 : 129 - 135
  • [8] New molecular determinant for inactivation of the human L-type α1C Ca2+ channel
    Soldatov, NM
    Zhenochin, S
    AlBanna, B
    Abernethy, DR
    Morad, M
    JOURNAL OF MEMBRANE BIOLOGY, 2000, 177 (02): : 129 - 135
  • [9] Construction of a vector for conditional gene targeting of the α1C subunit of the L-type CA-channel
    Specht, V
    Klugbauer, N
    Hofmann, F
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1998, 358 (01) : R163 - R163
  • [10] Role of the IIIS5-S6 linker of L-type Ca2+ channel α1C subunit in the action of Ca2+ channel agonist
    Yamaguchi, S
    Adachi-Akahane, S
    BIOPHYSICAL JOURNAL, 2002, 82 (01) : 103A - 103A