Phizicky David V, Bell Stephen P
Department of Biology, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, MA, USA.
Chromosoma. 2018 Dec;127(4):515-527. doi: 10.1007/s00412-018-0681-x. Epub 2018 Oct 1.
Execution of the meiotic and mitotic cell division programs requires distinct gene expression patterns. Unlike mitotic cells, meiotic cells reduce ploidy by following one round of DNA replication with two rounds of chromosome segregation (meiosis I and meiosis II). However, the mechanisms by which cells prevent DNA replication between meiosis I and meiosis II are not fully understood. Here, we show that transcriptional repression of two essential DNA replication genes, CDC6 and SLD2, is associated with production of shorter meiosis-specific RNAs containing the 3' end of both genes. Despite the short CDC6 RNA coding for a short protein (Cdc6), this protein is not essential for meiosis and it does not have either a positive or negative impact on DNA replication. Production of CDC6 mRNA does not require the upstream CDC6 promoter (P) and is not a processed form of the full-length RNA. Instead, CDC6 depends on transcription initiation from within the ORF upon repression of P. Finally, using CDC6 genes from related yeast, we show that repression of full-length CDC6 mRNA is evolutionarily conserved and that this repression is consistently associated with production of unique short CDC6 RNAs. Together, these data demonstrate that meiotic cells transcriptionally repress full-length CDC6 and SLD2, and that inactivation of P results in heterogeneous transcription initiation from within the CDC6 ORF.
减数分裂和有丝分裂细胞分裂程序的执行需要不同的基因表达模式。与有丝分裂细胞不同,减数分裂细胞通过一轮DNA复制后进行两轮染色体分离(减数分裂I和减数分裂II)来降低倍性。然而,细胞在减数分裂I和减数分裂II之间阻止DNA复制的机制尚未完全了解。在这里,我们表明,两个必需的DNA复制基因CDC6和SLD2的转录抑制与包含这两个基因3'端的较短减数分裂特异性RNA的产生有关。尽管短的CDC6 RNA编码一种短蛋白(Cdc6),但这种蛋白对减数分裂不是必需的,并且它对DNA复制没有正面或负面影响。CDC6 mRNA的产生不需要上游的CDC6启动子(P),也不是全长RNA的加工形式。相反,CDC6依赖于P被抑制后从开放阅读框内的转录起始。最后,使用来自相关酵母的CDC6基因,我们表明全长CDC6 mRNA的抑制在进化上是保守的,并且这种抑制始终与独特的短CDC6 RNA的产生相关。总之,这些数据表明减数分裂细胞转录抑制全长CDC6和SLD2,并且P的失活导致从CDC6开放阅读框内的异质转录起始。