Eaker S, Pyle A, Cobb J, Handel M A
Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, Knoxville, USA.
J Cell Sci. 2001 Aug;114(Pt 16):2953-65. doi: 10.1242/jcs.114.16.2953.
Mice heterozygous for Robertsonian centric fusion chromosomal translocations frequently produce aneuploid sperm. In this study RBJ/Dn x C57BL/6J F1 males, heterozygous for four Robertsonian translocations (2N=36), were analyzed to determine effects on germ cells of error during meiosis. Analysis of sperm by three color fluorescence in situ hybridization revealed significantly elevated aneuploidy, thus validating Robertsonian heterozygous mice as a model for production of chromosomally abnormal gametes. Primary spermatocytes from heterozygous males exhibited abnormalities of chromosome pairing in meiotic prophase and metaphase. In spite of prophase abnormalities, the prophase/metaphase transition occurred. However, an increased frequency of cells with misaligned condensed chromosomes was observed. Cytological analysis of both young and adult heterozygous mice revealed increased apoptosis in spermatocytes during meiotic metaphase I. Metaphase spermatocytes with misaligned chromosomes accounted for a significant proportion of the apoptotic spermatocytes, suggesting that a checkpoint process identifies aberrant meioses. Immunofluorescence staining revealed that kinetochores of chromosomes that failed to align on the spindle stained more intensely for kinetochore antigens CENP-E and CENP-F than did aligned chromosomes. Taken together, these observations are consistent with detection of malattached chromosomes by a meiotic spindle checkpoint mechanism that monitors attachment and/or congression of homologous chromosome pairs. However, the relatively high frequency of gametic aneuploidy suggests that the checkpoint mechanism does not efficiently eliminate all germ cells with chromosomal abnormalities.
罗伯逊氏着丝粒融合染色体易位的杂合子小鼠经常产生非整倍体精子。在本研究中,对RBJ/Dn×C57BL/6J F1雄性小鼠(对四种罗伯逊氏易位杂合,2N = 36)进行分析,以确定减数分裂过程中错误对生殖细胞的影响。通过三色荧光原位杂交对精子进行分析,结果显示非整倍体显著增加,从而验证了罗伯逊氏杂合子小鼠作为产生染色体异常配子模型的有效性。杂合子雄性的初级精母细胞在减数分裂前期和中期表现出染色体配对异常。尽管前期存在异常,但前期/中期转变仍会发生。然而,观察到染色体凝缩排列不齐的细胞频率增加。对幼年和成年杂合子小鼠的细胞学分析显示,减数分裂中期I的精母细胞凋亡增加。染色体排列不齐的中期精母细胞在凋亡精母细胞中占很大比例,这表明存在一个检查点过程来识别异常减数分裂。免疫荧光染色显示,未能在纺锤体上排列的染色体的动粒对比排列整齐的染色体的动粒抗原CENP - E和CENP - F染色更强烈。综上所述,这些观察结果与通过减数分裂纺锤体检查点机制检测染色体附着异常一致,该机制监测同源染色体对的附着和/或排列。然而,配子非整倍体的相对高频率表明,检查点机制不能有效地消除所有具有染色体异常的生殖细胞。