Vigodner Margarita, Ishikawa Tomomoto, Schlegel Peter N, Morris Patricia L
Center for Biomedical Research, Population Council, New York, New York, USA.
Am J Physiol Endocrinol Metab. 2006 May;290(5):E1022-33. doi: 10.1152/ajpendo.00527.2005. Epub 2005 Dec 13.
Sumoylation affects multiple cellular events, including chromatin inactivation and transcriptional repression. Our data provide the first characterization of small ubiquitin-related modifier-1 (SUMO-1) expression during human spermatogenesis by the use of high-resolution cellular SUMO-1 bioimaging. During human meiotic prophase, SUMO-1 localizes to sex chromosomes and centromeric and pericentromeric chromatin. As human spermatocytes progress toward the end of prophase in meiosis I, SUMO-1 is no longer detected within the sex body and pericentromeric heterochromatin but localizes exclusively to centromeres. SUMO-1 localization along sex chromosome axes, pseudoautosomal region, and centromeres of both chromosomes supports a role for SUMO-1 sumoylation in epigenetic events occurring over the entire sex body, e.g., meiotic sex chromosome inactivation and chromatin condensation. Centromeric SUMO-1 throughout meiotic prophase suggests a role in centromeric chromatin condensation and/or other centromere/kinetochore functions. SUMO-1 is likely involved in both facultative and constitutive heterochromatin processes in spermatocytes. Haploid round spermatids show a consistent association of SUMO-1 with centromeric clusters. During spermatid elongation, SUMO-1 localizes in the manchette perinuclear ring. Steroidogenic Leydig cells show some cytoplasmic but strong nuclear and perinuclear SUMO-1. Peritubular myoepithelial cell SUMO-1 colocalizes with centromeric heterochromatin. In epithelial Sertoli cells, when associated with centromeric heterochromatin, SUMO-1 is adjacent but not colocalized with the nucleolus. Male germ cells demonstrate no SUMO-1 nucleolar association. Human and rodent Sertoli cells consistently show an inverse correlation between androgen receptor (AR) and SUMO-1 expression and compartmentalization. Sertoli cells from certain infertile patients, however, showed greatly decreased SUMO-1 and AR. Our data suggest that human testicular SUMO-1 has specific functions in heterochromatin organization, meiotic centromere function, and gene expression.
小泛素相关修饰物1(SUMO-1)化影响多种细胞事件,包括染色质失活和转录抑制。我们的数据通过高分辨率细胞SUMO-1生物成像首次描述了人类精子发生过程中小泛素相关修饰物1(SUMO-1)的表达特征。在人类减数分裂前期,SUMO-1定位于性染色体以及着丝粒和着丝粒周围染色质。随着人类精母细胞向减数分裂I前期结束阶段发展,SUMO-1不再在性体和着丝粒周围异染色质中被检测到,而是仅定位于着丝粒。SUMO-1沿着性染色体轴、假常染色体区域以及两条染色体的着丝粒定位,这支持了SUMO-1化在整个性体发生的表观遗传事件中发挥作用,例如减数分裂性染色体失活和染色质浓缩。整个减数分裂前期着丝粒处的SUMO-1表明其在着丝粒染色质浓缩和/或其他着丝粒/动粒功能中发挥作用。SUMO-1可能参与精母细胞中的兼性和组成型异染色质过程。单倍体圆形精子细胞显示SUMO-1与着丝粒簇持续相关。在精子细胞伸长过程中,SUMO-1定位于核周环的袖套。类固醇生成的睾丸间质细胞显示出一些细胞质中的SUMO-1,但核内和核周的SUMO-1较强。睾丸支持细胞的SUMO-1与着丝粒异染色质共定位。在上皮性支持细胞中,当与着丝粒异染色质相关时,SUMO-1与核仁相邻但不共定位。雄性生殖细胞未显示SUMO-1与核仁相关。人类和啮齿动物的支持细胞始终显示雄激素受体(AR)与SUMO-1表达及分布之间呈负相关。然而,某些不育患者的支持细胞显示SUMO-1和AR大大减少。我们的数据表明,人类睾丸SUMO-1在异染色质组织、减数分裂着丝粒功能和基因表达中具有特定功能。