Wang D, Ikeda Y, Parker K L, Enders G C
Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City 66160-7400, USA.
Mol Reprod Dev. 1997 Oct;48(2):154-8. doi: 10.1002/(SICI)1098-2795(199710)48:2<154::AID-MRD2>3.0.CO;2-R.
The germ cell lineage is first recognized as a population of mitotically proliferating primordial germ cells that migrate toward the gonadal ridge. Shortly after arriving at the gonadal ridge, the germ cells begin to initiate a commitment to gamete production in the developing gonad. The mechanisms controlling this transition are poorly understood. We recently reported that a mouse germ cell nuclear antigen 1 (GCNA1) is initially detected in both male and female germ cells as they reach the gonad at 11.5 days postcoitum (dpc). GCNA1 is continually expressed in germ cells through all stages of gametogenesis until the diplotene/dictyate stage of meiosis I. Since GCNA1 expression commences soon after primordial germ cells arrive at the gonadal ridge, we wanted to determine whether the gonadal environment was essential for induction of GCNA1 expression. By examining GCNA1 expression in germ cells that migrate ectopically into the adrenal gland, we determined that both the gonadal and adrenal gland environments allow GCNA1 expression. We also examined GCNA1 expression Ftz-F1 null mice, which were born lacking gonads and adrenal glands. During embryonic development in the Ftz-F1 null mice, the gonad and most germ cells undergo apoptotic degeneration at about 12.5 dpc. While most of the germ cells undergo apoptosis without expressing GCNA1, a few surviving germs cells, especially outside the involuting gonad clearly express GCNA1. Thus, although the Ftz-F1 gene is essential for gonadal and adrenal development, induction of GCNA1 expression in germ cells does not require Ftz-F1 gene products. The finding that germ cell GCNA1 expression is not restricted to the gonadal environment and is not dependent on the Ftz-F1 gene products suggests that GCNA1 expression may be initiated in the germ cell lineage by autonomous means.
生殖细胞谱系最初被识别为一群进行有丝分裂增殖的原始生殖细胞,它们向性腺嵴迁移。到达性腺嵴后不久,生殖细胞开始在发育中的性腺中启动向配子产生的定向分化。控制这种转变的机制目前了解甚少。我们最近报道,小鼠生殖细胞核抗原1(GCNA1)最初在雄性和雌性生殖细胞中被检测到,此时它们在交配后11.5天(dpc)到达性腺。GCNA1在生殖细胞的整个配子发生阶段持续表达,直至减数分裂I的双线期/核网期。由于GCNA1的表达在原始生殖细胞到达性腺嵴后不久就开始了,我们想确定性腺环境对于GCNA1表达的诱导是否至关重要。通过检查异位迁移到肾上腺的生殖细胞中GCNA1的表达,我们确定性腺和肾上腺环境都允许GCNA1表达。我们还检查了Ftz-F1基因敲除小鼠中GCNA1的表达,这些小鼠出生时缺乏性腺和肾上腺。在Ftz-F1基因敲除小鼠的胚胎发育过程中,性腺和大多数生殖细胞在大约12.5 dpc时发生凋亡性退化。虽然大多数生殖细胞在不表达GCNA1的情况下发生凋亡,但一些存活的生殖细胞,特别是在退化性腺外部的细胞明显表达GCNA1。因此,尽管Ftz-F1基因对于性腺和肾上腺的发育至关重要,但生殖细胞中GCNA1表达的诱导并不需要Ftz-F1基因产物。生殖细胞GCNA1表达不限于性腺环境且不依赖于Ftz-F1基因产物这一发现表明,GCNA1的表达可能通过自主方式在生殖细胞谱系中启动。