Mankertz Annette, Caliskan Rifat, Hattermann Kim, Hillenbrand Bernd, Kurzendoerfer Petra, Mueller Bettina, Schmitt Cornelia, Steinfeldt Tobias, Finsterbusch Tim
P24 (Xenotransplantation), Robert Koch-Institut, Nordufer 20, 13353 Berlin, Germany.
Vet Microbiol. 2004 Feb 4;98(2):81-8. doi: 10.1016/j.vetmic.2003.10.014.
The rep gene of Porcine circovirus type 1 directs the synthesis of two proteins. The full-length protein Rep is 312 amino acids in size, the spliced variant Rep' is truncated (168 aa) and exon 2 is frame-shifted. Replication of PCV1 DNA depends on synthesis of both proteins. Rep and Rep' bind in vitro to double-stranded DNA fragments comprising part of the origin of replication of PCV1, but the minimal binding sites of the two proteins are distinct. Rep protein represses the promoter of the rep gene by binding to the two inner hexamers H1 and H2. Although Rep' binds to the same sequence, it does not influence Prep. Twelve hours after PCV1 infection, similar amounts of rep and rep' were detected by real-time PCR, but later on, the ratio of the two transcripts varied. Both proteins are co-localised in the nucleus and formation of homo- and heteromeric complexes has been observed. When a replication assay was performed, in which Rep and Rep' protein of PCV1 was used to replicate the origin of PCV1 and PCV2, the rep gene products were found to initiate replication at both origins of replication.
猪圆环病毒1型的rep基因指导合成两种蛋白质。全长蛋白Rep大小为312个氨基酸,剪接变体Rep'被截短(168个氨基酸)且外显子2发生移码。PCV1 DNA的复制依赖于这两种蛋白质的合成。Rep和Rep'在体外与包含PCV1复制起点一部分的双链DNA片段结合,但这两种蛋白质的最小结合位点不同。Rep蛋白通过与两个内部六聚体H1和H2结合来抑制rep基因的启动子。尽管Rep'与相同序列结合,但它不影响Prep。PCV1感染12小时后,通过实时PCR检测到rep和rep'的量相似,但随后,这两种转录本的比例发生变化。这两种蛋白质都共定位于细胞核中,并且已观察到同型和异型复合物的形成。当进行复制试验时,其中使用PCV1的Rep和Rep'蛋白来复制PCV1和PCV2的起点,发现rep基因产物在两个复制起点处均启动复制。