Vernet Nadege, Mahadevaiah Shantha K, Decarpentrie Fanny, Longepied Guy, de Rooij Dirk G, Burgoyne Paul S, Mitchell Michael J
Division of Developmental Genetics, MRC National Institute for Medical Research, London, United Kingdom.
Department of Functional Genomics and Cancer, Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch Cedex, France.
PLoS One. 2016 Jan 14;11(1):e0145398. doi: 10.1371/journal.pone.0145398. eCollection 2016.
A previous study indicated that genetic information encoded on the mouse Y chromosome short arm (Yp) is required for efficient completion of the second meiotic division (that generates haploid round spermatids), restructuring of the sperm head, and development of the sperm tail. Using mouse models lacking a Y chromosome but with varying Yp gene complements provided by Yp chromosomal derivatives or transgenes, we recently identified the Y-encoded zinc finger transcription factors Zfy1 and Zfy2 as the Yp genes promoting the second meiotic division. Using the same mouse models we here show that Zfy2 (but not Zfy1) contributes to the restructuring of the sperm head and is required for the development of the sperm tail. The preferential involvement of Zfy2 is consistent with the presence of an additional strong spermatid-specific promotor that has been acquired by this gene. This is further supported by the fact that promotion of sperm morphogenesis is also seen in one of the two markedly Yp gene deficient models in which a Yp deletion has created a Zfy2/1 fusion gene that is driven by the strong Zfy2 spermatid-specific promotor, but encodes a protein almost identical to that encoded by Zfy1. Our results point to there being further genetic information on Yp that also has a role in restructuring the sperm head.
先前的一项研究表明,小鼠Y染色体短臂(Yp)上编码的遗传信息对于有效完成第二次减数分裂(产生单倍体圆形精子细胞)、精子头部的重塑以及精子尾部的发育是必需的。利用缺乏Y染色体但具有由Yp染色体衍生物或转基因提供的不同Yp基因互补的小鼠模型,我们最近确定了Y编码的锌指转录因子Zfy1和Zfy2是促进第二次减数分裂的Yp基因。利用相同的小鼠模型,我们在此表明Zfy2(而非Zfy1)有助于精子头部的重塑,并且是精子尾部发育所必需的。Zfy2的优先参与与该基因获得的一个额外的强大精子细胞特异性启动子的存在相一致。这一事实进一步支持了这一点,即在两个明显的Yp基因缺陷模型之一中也观察到了精子形态发生的促进,在该模型中,Yp缺失产生了一个由强大的Zfy2精子细胞特异性启动子驱动的Zfy2/1融合基因,但编码的蛋白质几乎与Zfy1编码的蛋白质相同。我们的结果表明,Yp上还有其他遗传信息在精子头部重塑中也发挥作用。