PKD2 cation channel is required for directional sperm movement and male fertility

被引:63
作者
Gao, ZQ [1 ]
Ruden, DM [1 ]
Lu, XY [1 ]
机构
[1] Univ Alabama, Dept Environm Hlth Sci, Birmingham, AL 35294 USA
关键词
D O I
10.1016/j.cub.2003.11.053
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
Sperm of both mammals and invertebrates move toward specific sites in the female reproductive tract. However, molecular mechanisms for sperm to follow directional cues are unknown. Here, we report genetic analysis of Drosophila Pkd2 at 33E3 (Pkd2, CG6504) which encodes a Ca2+-activated, nonselective cation channel homologous to the human Pkd2 autosomal dominant polycystic kidney disease (ADPKD) gene [1]. The PKD2 family of genes has been implicated in sensory responses through protein localization on primary cilia of epithelia and neurons [2-4]. In renal tubules, cilium-associated PKD2 appears to mediate Ca2+ influx in response to fluid flow, and the loss of fluid sensation probably contributes to cyst growth and ADPKD [4]. Sperm tails or flagella are specialized cilia essential for movement. Drosophila Pkd2 is abundantly associated with the tail and the acrosome-containing head region of mature sperm. Targeted disruption of Pkd2 results in male sterility without affecting spermatogenesis. The mutant sperm are motile but fail to swim into the storage organs in the female. Rare mutant sperm that reach the storage organs are able to fertilize the egg and produce viable progeny. Our data demonstrate that the Drosophila PKD2 cation channel operates in sperm for directional movement inside the female reproductive tract.
引用
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页码:2175 / 2178
页数:4
相关论文
共 16 条
  • [1] The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway
    Barr, MM
    DeModena, J
    Braun, D
    Nguyen, CQ
    Hall, DH
    Sternberg, PW
    [J]. CURRENT BIOLOGY, 2001, 11 (17) : 1341 - 1346
  • [2] SPERM CHEMOTAXIS - EGG PEPTIDES CONTROL CYTOSOLIC CALCIUM TO REGULATE FLAGELLAR RESPONSES
    COOK, SP
    BROKAW, CJ
    MULLER, CH
    BABCOCK, DF
    [J]. DEVELOPMENTAL BIOLOGY, 1994, 165 (01) : 10 - 19
  • [3] Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel
    González-Perrett, S
    Kim, K
    Ibarra, C
    Damiano, AE
    Zotta, E
    Batelli, M
    Harris, PC
    Reisin, IL
    Arnaout, MA
    Cantiello, HF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (03) : 1182 - 1187
  • [4] Identification of a human homologue of the sea urchin receptor for egg jelly: a polycystic kidney disease-like protein
    Hughes, J
    Ward, CJ
    Aspinwall, R
    Butler, R
    Harris, PC
    [J]. HUMAN MOLECULAR GENETICS, 1999, 8 (03) : 543 - 549
  • [5] Identification and characterization of the major Drosophila melanogaster mating plug protein
    Lung, O
    Wolfner, MF
    [J]. INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2001, 31 (6-7) : 543 - 551
  • [6] Two populations of node monocilia initiate left-right asymmetry in the mouse
    McGrath, J
    Somlo, S
    Makova, S
    Tian, X
    Brueckner, M
    [J]. CELL, 2003, 114 (01) : 61 - 73
  • [7] suREJ3, a polycystin-1 protein, is cleaved at the GPS domain and localizes to the acrosomal region of sea urchin sperm
    Mengerink, KJ
    Moy, GW
    Vacquier, VD
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (02) : 943 - 948
  • [8] Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells
    Nauli, SM
    Alenghat, FJ
    Luo, Y
    Williams, E
    Vassilev, P
    Lil, XG
    Elia, AEH
    Lu, WN
    Brown, EM
    Quinn, SJ
    Ingber, DE
    Zhou, J
    [J]. NATURE GENETICS, 2003, 33 (02) : 129 - 137
  • [9] Neubaum DM, 1999, GENETICS, V153, P845
  • [10] The developments between gametogenesis and fertilization:: ovulation and female sperm storage in Drosophila melanogaster
    Qazi, MCB
    Heifetz, Y
    Wolfner, MF
    [J]. DEVELOPMENTAL BIOLOGY, 2003, 256 (02) : 195 - 211