Banerjee Amrita, Roy Somnath, Tarafdar Jayanta
Department of Plant Pathology, BCKV, Mohanpur, Nadia 741252, West Bengal, India.
Virus Genes. 2012 Apr;44(2):312-8. doi: 10.1007/s11262-011-0680-y. Epub 2011 Oct 12.
Rice tungro bacilliform virus (RTBV) is a plant pararetrovirus. The large intergenic region (LIGR) of RTBV having a single transcriptional promoter produces more than genome length pregenomic RNA (pgRNA) which directs synthesis of circular double-stranded viral DNA and serves as a polycistronic mRNA. By computer-aided analysis of LIGR, the 11 RTBV isolates sequenced so far were compared with respect to structural organization of promoter and pgRNA 5'-leader. The results revealed only 74.90% identity at LIGR between 'Southeast Asian' (SEA) and 'South Asian' (SA) isolates of RTBV indicating considerable variation between two groups which was also reflected during analysis of promoter and leader sequence. The predicted promoter region of SA isolates exhibited major variations in terms of transcription start site and consensus sequences of cis motifs expecting further exploitation of promoter region of SA isolates. The reduced length of leader sequence along with less numbers and different arrangements of small open reading frames (sORFs) in case of SA isolates might have some alterations in the control of expression of ORF II and III between the two groups. In spite of these variations, the leader sequence of both SEA and SA type isolates showed formation of stable secondary or stem-loop structure having identical features for efficient translation. The conservation of sORF1 at seven nucleotides upstream of stable stem-loop, CU-rich sequence following the sORF1 stop codon and AU-rich shunt landing sequence immediately downstream of the secondary structure suggested conservation of ribosomal shunt mechanism in all RTBV isolates irrespective of their geographical distribution.
水稻东格鲁杆状病毒(RTBV)是一种植物类逆转录病毒。RTBV的大基因间隔区(LIGR)具有单一转录启动子,可产生超过基因组长度的前基因组RNA(pgRNA),该RNA指导环状双链病毒DNA的合成,并作为多顺反子mRNA。通过对LIGR的计算机辅助分析,将目前已测序的11个RTBV分离株在启动子和pgRNA 5'前导序列的结构组织方面进行了比较。结果显示,RTBV的“东南亚”(SEA)分离株和“南亚”(SA)分离株在LIGR处的同一性仅为74.90%,表明两组之间存在相当大的差异,这在启动子和前导序列分析中也有所体现。SA分离株的预测启动子区域在转录起始位点和顺式基序的共有序列方面表现出主要差异,有望对SA分离株的启动子区域进行进一步研究。SA分离株前导序列长度缩短,小开放阅读框(sORF)数量减少且排列不同,这可能导致两组之间ORF II和III表达调控的某些改变。尽管存在这些差异,SEA和SA型分离株的前导序列均显示形成了具有相同特征的稳定二级或茎环结构,以实现高效翻译。稳定茎环上游七个核苷酸处sORF1的保守性、sORF1终止密码子后的富含CU序列以及二级结构下游紧邻的富含AU的分流着陆序列表明,所有RTBV分离株无论其地理分布如何,核糖体分流机制均具有保守性。