Oral-aboral axis specification in the sea urchin embryo -: II.: Mitochondrial distribution and redox state contribute to establishing polarity in Strongylocentrotus purpuratus

被引:76
作者
Coffman, JA [1 ]
McCarthy, JJ [1 ]
Dickey-Sims, C [1 ]
Robertson, AJ [1 ]
机构
[1] Stowers Inst Med Res, Kansas City, MO 64110 USA
关键词
sea urchin; development; mitochondria; redox state; transcription; metabolic gradient;
D O I
10.1016/j.ydbio.2004.06.005
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The initial asymmetry that specifies the oral-aboral (OA) axis of the sea urchin embryo has long been a mystery. It was shown previously that OA polarity can be entrained in embryos by imposing a respiratory asymmetry, with the most oxidizing side of the embryo tending to develop as the oral pole. This suggests that one of the earliest observable asymmetries along the incipient OA axis, a redox gradient established by a higher density and/or activity of mitochondria on the prospective oral side of the embryo, might play a causal role in establishing the axis. Here, we examine the origin and functional significance of this early redox gradient. Using MitoTracker Green, we show that mitochondria are asymmetrically distributed in the unfertilized egg of Strongylocentrotus purpuratus, and that the polarity of the maternal asymmetry is maintained in the zygote. Vital staining indicates that the side of the embryo that inherits the highest density of mitochondria tends to develop into the oral pole. This correlation holds when mitochondria are redistributed by centrifugation of eggs or by transfer of purified mitochondria into zygotes, indicating that an asymmetric mitochondrial distribution can entrain OA polarity, possibly through effects on intracellular redox state. In support of this possibility, we find that specification of oral ectoderm is suppressed when embryos are cultured under hypoxic conditions that enforce a relatively reducing redox state. This effect is reversed by overexpression of nodal, an early zygotic marker of oral specification whose localized expression suffices to organize the entire OA axis, indicating that redox state is upstream of nodal expression. We therefore propose that a threshold level of intracellular oxidation is required to effectively activate nodal, and that precocious attainment of this threshold within the blastomeres containing the highest density of mitochondria results in asymmetric nodal activity and consequent specification of the OA axis. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:160 / 171
页数:12
相关论文
共 38 条
[1]   Redox regulation of the DNA binding activity in transcription factor PEBP2 - The roles of two conserved cysteine residues [J].
Akamatsu, Y ;
Ohno, T ;
Hirota, K ;
Kagoshima, H ;
Yodoi, J ;
Shigesada, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (23) :14497-14500
[2]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[3]   Spdeadringer, a sea urchin embryo gene required separately in skeletogenic and oral ectoderm gene regulatory networks [J].
Amore, G ;
Yavrouian, RG ;
Peterson, KJ ;
Ransick, A ;
McClay, DR ;
Davidson, EH .
DEVELOPMENTAL BIOLOGY, 2003, 261 (01) :55-81
[4]   Patterning the sea urchin embryo: Gene regulatory networks, signaling pathways, and cellular interactions [J].
Angerer, LM ;
Angerer, RC .
CURRENT TOPICS IN DEVELOPMENTAL BIOLOGY, VOL 53, 2003, 53 :159-198
[5]  
Angerer LM, 2001, DEVELOPMENT, V128, P4393
[6]  
Blackstone NW, 1999, J EXP BIOL, V202, P3541
[7]  
Calzone FJ, 1997, MOL MAR BIOL BIOTECH, V6, P79
[8]  
CAMERON RA, 1989, DEVELOPMENT, V106, P641
[9]   EXOGASTRULATION BY SODIUM AZIDE AND OTHER INHIBITING CONDITIONS IN STRONGYLOCENTROTUS PURPURATUS [J].
CHILD, CM .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1948, 107 (01) :1-38
[10]   Cooperation of protein disulfide isomerase and redox environment in the regulation of NF-kappa B and AP1 binding to DNA [J].
Clive, DR ;
Greene, JJ .
CELL BIOCHEMISTRY AND FUNCTION, 1996, 14 (01) :49-55