H1foo is indispensable for meiotic maturation of the mouse oocyte

被引:44
作者
Furuya, Masataka
Tanaka, Mamoru [1 ]
Teranishi, Takahide
Matsumoto, Kazuya
Hosoi, Yoshihiko
Saeki, Kazuhiro
Ishimoto, Hitoshi
Minegishi, Kazuhiro
Iritani, Akira
Yoshimura, Yasunori
机构
[1] Keio Univ, Sch Med, Dept Obstet & Gynecol, Tokyo 1608582, Japan
[2] Ota Gen Hosp, Dept Obstet & Gynecol, Ota 3738585, Japan
[3] Kinki Univ, Grad Sch Biol Oriented Sci & Technol, Div Biol Sci, Wakayama 6496493, Japan
关键词
H1foo; linker histone; meiotic maturation; morpholino; mouse; oocyte;
D O I
10.1262/jrd.19008
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Oocyte-specific linker histone H1foo is localized in the oocyte nucleus, either diffusely or bound to chromatin, during the processes of meiotic maturation and fertilization. This expression pattern suggests that H1foo plays a key role in the control of gene expression and chromatin modification during oogenesis and early embryogenesis. To reveal the function of H1foo, we microinjected antisense morpholino oligonucleotides (MO) against H1foo into mouse germinal-vesicle stage oocytes. The rate of in vitro maturation of the antisense MO group was significantly lower than that of the control group. Eggs that failed to extrude a first polar body following injection of antisense MO arrested at metaphase I. Additionally, co-injection of in vitro synthesized H1foo mRNA along with antisense MO successfully rescued expression of H1foo and improved the in vitro maturation rate. There was no difference in the rate of parthenogenesis between the antisense MO and control groups. These results indicate that H1foo is essential for maturation of germinal vesicle-stage oocytes.
引用
收藏
页码:895 / 902
页数:8
相关论文
共 32 条
[1]   Histone H1 is dispensable for methylation-associated gene silencing in Ascobolus immersus and essential for long life span [J].
Barra, JL ;
Rhounim, L ;
Rossignol, JL ;
Faugeron, G .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (01) :61-69
[2]   Differential in vivo binding dynamics of somatic and oocyte-specific linker histones in oocytes and during ES cell nuclear transfer [J].
Becker, M ;
Becker, A ;
Miyara, F ;
Han, ZM ;
Kihara, M ;
Brown, DT ;
Hager, GL ;
Latham, K ;
Adashi, EY ;
Misteli, T .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (08) :3887-3895
[3]   Differential effect of H1 variant overexpression on cell cycle progression and gene expression [J].
Brown, DT ;
Alexander, BT ;
Sittman, DB .
NUCLEIC ACIDS RESEARCH, 1996, 24 (03) :486-493
[4]  
CHOI T, 1991, DEVELOPMENT, V113, P789
[5]   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
[6]   Histones: Genetic diversity and tissue-specific gene expression [J].
Doenecke, D ;
Albig, W ;
Bode, C ;
Drabent, B ;
Franke, K ;
Gavenis, K ;
Witt, O .
HISTOCHEMISTRY AND CELL BIOLOGY, 1997, 107 (01) :1-10
[7]   Suppression of homologous recombination by the Saccharomyces cerevisiae linker histone [J].
Downs, JA ;
Kosmidou, E ;
Morgan, A ;
Jackson, SP .
MOLECULAR CELL, 2003, 11 (06) :1685-1692
[8]   THE MATERNAL HISTONE H1 VARIANT, H1M (B4 PROTEIN), IS THE PREDOMINANT H1 HISTONE IN XENOPUS-PREGASTRULA EMBRYOS [J].
DWORKINRASTL, E ;
KANDOLF, H ;
SMITH, RC .
DEVELOPMENTAL BIOLOGY, 1994, 161 (02) :425-439
[9]   H1 linker histories are essential for mouse development and affect nucleosome spacing in vivo [J].
Fan, YH ;
Nikitina, T ;
Morin-Kensicki, EM ;
Zhao, J ;
Magnuson, TR ;
Woodcock, CL ;
Skoultchi, AI .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (13) :4559-4572
[10]   Individual somatic H1 subtypes are dispensable for mouse development even in mice lacking the H1° replacement subtype [J].
Fan, YH ;
Sirotkin, A ;
Russell, RG ;
Ayala, J ;
Skoultchi, AI .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (23) :7933-7943