TACC3 expression and localization in the murine egg and ovary

被引:26
作者
Hao, ZL
Stoler, MH
Sen, B
Shore, A
Westbrook, A
Flickinger, CJ
Herr, JC [1 ]
Coonrod, SA
机构
[1] Univ Virginia, Dept Cell Biol, Ctr Recombinant Gamete Contracept Vaccinogens, Charlottesville, VA 22908 USA
[2] Univ Virginia, Ctr Recombinant Gamete Immunocontracept Vaccinoge, Charlottesville, VA 22908 USA
[3] Univ Virginia, Dept Pathol, Charlottesville, VA 22903 USA
关键词
cellular localization; oocyte; proteomics; TACC3; tissue distribution;
D O I
10.1002/mrd.90012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
A protein spot cored from a silver-stained two dimensional (2D) gel of germinal vesicle stage immature mouse oocytes was identified as Transforming Acidic Coiled Coil containing protein (TACC3) by tandem mass spectrometry. PCR amplification revealed two alternatively spliced forms, Tacc3a and Tacc3b, in mouse ovarian cDNA libraries. TACC3a encoded a 630 aa protein with a predicted mass of 70 kDa. It contained seven 24 aa repeats at the N-terminus and two coiled-coil domains at the C-terminus. TACC3b encoded a 426 aa protein with a predicted mass of 49 kDa also containing two coiled coil domains, but lacking the 168 aa repeat region. In addition to homology to the TACC family members, murine TACC3 also showed 35.7% identity to the Xenopus protein, Maskin, a cytoplasmic polyadenylation element binding protein (CPEB)-associated factor. Northern blot analysis demonstrated that TACC3a is abundantly expressed in adult testis and spleen and is moderately expressed in the ovary, heart, and lung, suggesting a wide tissue distribution. Both myc-tagged TACC3a and TACC3b targeted to the cytoplasm of transiently transfected CV-1 cells. In situ hybridization of mouse ovarian tissue sections displayed abundant expression of TACC3 specifically in the cytoplasm of growing oocytes, but not in primordial or atretic follicles. This pattern of expression suggests that TACC3 is expressed in ovarian cells undergoing active growth and development.
引用
收藏
页码:291 / 299
页数:9
相关论文
共 28 条
[1]
Proteomics: applications in basic and applied biology [J].
Anderson, NL ;
Matheson, AD ;
Steiner, S .
CURRENT OPINION IN BIOTECHNOLOGY, 2000, 11 (04) :408-412
[2]
ANGERER LM, 1987, IN SITU HYBRIDIZATIO, P42
[3]
Proteomics: the next step after genomics? [J].
Bradbury, J .
LANCET, 2000, 356 (9223) :50-50
[4]
Proteomics in reproductive research - The potential importance of proteomics to research in reproduction [J].
Brewis, IA .
HUMAN REPRODUCTION, 1999, 14 (12) :2927-2929
[5]
AZU-1:: A candidate breast tumor suppressor and biomarker for tumor progression [J].
Chen, HM ;
Schmeichel, KL ;
Mian, IS ;
Lelièvre, S ;
Petersen, OW ;
Bissell, MJ .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (04) :1357-1367
[6]
Oolemmal proteomics [J].
Coonrod, SA ;
Wright, PW ;
Herr, JC .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2002, 53 (1-2) :55-65
[7]
A morpholino phenocopy of the mouse mos mutation [J].
Coonrod, SA ;
Bolling, LC ;
Wright, PW ;
Visconti, PE ;
Herr, JC .
GENESIS, 2001, 30 (03) :198-200
[8]
Control of mRNA stability and translation during Drosophila development [J].
Cooperstock, RL ;
Lipshitz, HD .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 1997, 8 (06) :541-549
[9]
Control of cell lineage-specific development and transcription by bHLH-PAS proteins [J].
Crews, ST .
GENES & DEVELOPMENT, 1998, 12 (05) :607-620
[10]
D-TACC:: a novel centrosomal protein required for normal spindle function in the early Drosophila embryo [J].
Gergely, F ;
Kidd, D ;
Jeffers, K ;
Wakefield, JG ;
Raff, JW .
EMBO JOURNAL, 2000, 19 (02) :241-252