Penkner Alexandra M, Fridkin Alexandra, Gloggnitzer Jiradet, Baudrimont Antoine, Machacek Thomas, Woglar Alexander, Csaszar Edina, Pasierbek Pawel, Ammerer Gustav, Gruenbaum Yosef, Jantsch Verena
Department of Chromosome Biology, Max F. Perutz Laboratories, University of Vienna, 1030-Vienna, Austria.
Cell. 2009 Nov 25;139(5):920-33. doi: 10.1016/j.cell.2009.10.045. Epub 2009 Nov 12.
Genome haploidization during meiosis depends on recognition and association of parental homologous chromosomes. The C. elegans SUN/KASH domain proteins Matefin/SUN-1 and ZYG-12 have a conserved role in this process. They bridge the nuclear envelope, connecting the cytoplasm and the nucleoplasm to transmit forces that allow chromosome movement and homolog pairing and prevent nonhomologous synapsis. Here, we show that Matefin/SUN-1 forms rapidly moving aggregates at putative chromosomal attachment sites in the meiotic transition zone (TZ). We analyzed requirements for aggregate formation and identified multiple phosphotarget residues in the nucleoplasmic domain of Matefin/SUN-1. These CHK-2 dependent phosphorylations occur in leptotene/zygotene, diminish during pachytene and are involved in pairing. Mimicking phosphorylation causes an extended TZ and univalents at diakinesis. Our data suggest that the properties of the nuclear envelope are altered during the time window when homologs are sorted and Matefin/SUN-1 aggregates form, thereby controling the movement, homologous pairing and interhomolog recombination of chromosomes.
减数分裂过程中的基因组单倍体化依赖于亲本同源染色体的识别和配对。秀丽隐杆线虫的SUN/KASH结构域蛋白Matefin/SUN-1和ZYG-12在此过程中发挥着保守作用。它们跨越核膜,连接细胞质和核质以传递力量,从而促进染色体移动、同源配对并防止非同源联会。在此,我们发现Matefin/SUN-1在减数分裂过渡区(TZ)的假定染色体附着位点形成快速移动的聚集体。我们分析了聚集体形成的条件,并在Matefin/SUN-1的核质结构域中鉴定出多个磷酸化靶点残基。这些依赖CHK-2的磷酸化发生在细线期/偶线期,在粗线期减少,并参与配对过程。模拟磷酸化会导致延长的TZ和终变期单价体。我们的数据表明,在同源染色体分类和Matefin/SUN-1聚集体形成的时间窗口内,核膜的性质发生了改变,从而控制染色体移动、同源配对和同源染色体间重组。