Gómez Rocío, Felipe-Medina Natalia, Ruiz-Torres Miguel, Berenguer Inés, Viera Alberto, Pérez Sara, Barbero José Luis, Llano Elena, Fukuda Tomoyuki, Alsheimer Manfred, Pendás Alberto M, Losada Ana, Suja José A
Unidad de Biología Celular, Departamento de Biología, Facultad de Ciencias, Universidad Autónoma de Madrid, Madrid, Spain
Instituto de Biología Molecular y Celular del Cáncer (CSIC-Universidad de Salamanca) Campus Miguel de Unamuno, Salamanca, Spain.
EMBO Rep. 2016 May;17(5):695-707. doi: 10.15252/embr.201541060. Epub 2016 Mar 7.
The distribution and regulation of the cohesin complexes have been extensively studied during mitosis. However, the dynamics of their different regulators in vertebrate meiosis is largely unknown. In this work, we have analyzed the distribution of the regulatory factor Sororin during male mouse meiosis. Sororin is detected at the central region of the synaptonemal complex during prophase I, in contrast with the previously reported localization of other cohesin components in the lateral elements. This localization of Sororin depends on the transverse filaments protein SYCP1, but not on meiosis-specific cohesin subunits REC8 and SMC1β. By late prophase I, Sororin accumulates at centromeres and remains there up to anaphase II The phosphatase activity of PP2A seems to be required for this accumulation. We hypothesize that Sororin function at the central region of the synaptonemal complex could be independent on meiotic cohesin complexes. In addition, we suggest that Sororin participates in the regulation of centromeric cohesion during meiosis in collaboration with SGO2-PP2A.
在有丝分裂过程中,黏连蛋白复合体的分布与调控已得到广泛研究。然而,在脊椎动物减数分裂中,其不同调控因子的动态变化在很大程度上仍不清楚。在这项研究中,我们分析了调控因子Sororin在雄性小鼠减数分裂过程中的分布。在减数第一次分裂前期,Sororin定位于联会复合体的中央区域,这与之前报道的其他黏连蛋白成分定位于侧生元件不同。Sororin的这种定位依赖于横向丝蛋白SYCP1,但不依赖于减数分裂特异性黏连蛋白亚基REC8和SMC1β。到减数第一次分裂前期晚期,Sororin在着丝粒处积累,并一直持续到减数第二次分裂后期。PP2A的磷酸酶活性似乎是这种积累所必需的。我们推测,Sororin在联会复合体中央区域的功能可能独立于减数分裂黏连蛋白复合体。此外,我们认为Sororin在减数分裂过程中与SGO2-PP2A协同参与着丝粒黏连的调控。