首页> 美国卫生研究院文献>Journal of Virology >Mareks disease virus latency-associated transcripts belong to a family of spliced RNAs that are antisense to the ICP4 homolog gene.
【2h】

Mareks disease virus latency-associated transcripts belong to a family of spliced RNAs that are antisense to the ICP4 homolog gene.

机译:马立克氏病病毒潜伏期相关的转录物属于一个与ICP4同源基因反义的剪接RNA家族。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Marek's disease virus (MDV) latency-associated transcripts include at least two MDV small RNAs (MSRs) and a 10-kb RNA which map antisense to the ICP4 homolog gene and are relatively abundant in MDV-transformed lymphoblastoid cells. This report further describes the biological and structural properties of these RNAs. First, these RNAs were detected in primary lymphomas isolated from chickens infected with several oncogenic MDV strains. Second, the MSRs are nonpolyadenylated, whereas, the 10-kb RNA is predominantly polyadenylated. Third, MSRs localize to the nuclei of both lymphoblastoid cells and cytolytically infected chicken embryo fibroblasts. Fourth, the 3'-region splice junctions of the MSRs during latent and productive infection were determined by sequencing RNA-PCR products generated with primers that flank the 3' splice region. The MSRs contain at least three introns, the largest of which overlaps the ICP4 putative translational start site. Fifth, the 5' end of the MSRs initiates approximately 5 kb upstream from the main body of the RNA. The extreme 5' exon is approximately 251 nucleotides (nt) long and is joined to the main body of the transcript upon removal of a 4,852-nt intron. Finally, the 10-kb RNA lies entirely within the repeats flanking the unique short region of the genome. We believe that the MSRs and 10-kb RNA belong to a family of spliced RNAs that map antisense to the ICP4 gene and comprise a complex transcriptional unit expressed during MDV-induced T-cell transformation.
机译:马立克氏病病毒(MDV)潜伏期相关的转录本包括至少两个MDV小RNA(MSR)和一个10 kb RNA,它们将反义图谱映射到ICP4同源基因,并且在MDV转化的淋巴母细胞中相对丰富。该报告进一步描述了这些RNA的生物学和结构特性。首先,在分离自感染了几种致癌MDV株的鸡的原发性淋巴瘤中检测到这些RNA。其次,MSR是非聚腺苷酸化的,而10-kb RNA主要是聚腺苷酸化的。第三,MSRs定位于淋巴母细胞和细胞溶解感染的鸡胚成纤维细胞的核中。第四,在潜伏性感染和生产性感染过程中,MSR的3'-区域剪接点通过对RNA-PCR产物进行测序来确定,该产物由位于3'-剪接区域侧翼的引物产生。 MSR包含至少三个内含子,其中最大内含子与ICP4假定的翻译起始位点重叠。第五,MSR的5'末端起始于RNA主体上游约5 kb。极端的5'外显子长约251个核苷酸(nt),并在除去4,852-nt内含子后与转录本的主体连接。最后,10 kb RNA完全位于基因组独特短区两侧的重复序列中。我们相信,MSR和10-kb RNA属于剪接RNA家族,其将反义图谱映射到ICP4基因,并包含在MDV诱导的T细胞转化过程中表达的复杂转录单位。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号