Haffar A, Libeau G, Moussa A, Cécile M, Diallo A
Département d'Elevage et de Médecine Vétérinaire, Cirad-emvt, Campus International de Baillarguet, 34032 Montellier, BP 5035, Montpellier, France.
Virus Res. 1999 Oct;64(1):69-75. doi: 10.1016/s0168-1702(99)00080-5.
The gene encoding the matrix protein of peste des petits ruminants virus (PPRV) has been cloned and its nucleotide sequence determined. This gene is 1466 nucleotides long and contains an open reading frame (ORF) capable of encoding a basic protein of 335 amino acid residues with a predicted molecular weight of 38,057 Da. This ORF starts at position 33-35 and ends with the codon TAA at position 1038-1040 thus leaving a long untranslated region (426 nucleotides) at the 3' end of the messenger RNA. This fragment is very G/C rich (68.5%) and in contrast to the ORF region appears to be least conserved in the M gene sequence of the morbilliviruses. A comparison of the PPRV M protein with those of other viruses in the group confirms the previously noted high degree of conservation for this protein sequence. The percent of identity within the group ranges from 76.7 to 86.9%, the highest being with the dolphin morbillivirus matrix protein.
小反刍兽疫病毒(PPRV)基质蛋白的编码基因已被克隆并测定了其核苷酸序列。该基因长度为1466个核苷酸,包含一个开放阅读框(ORF),能够编码一个由335个氨基酸残基组成的碱性蛋白,预测分子量为38,057道尔顿。这个开放阅读框从第33 - 35位开始,以第1038 - 1040位的TAA密码子结束,因此在信使RNA的3'端留下了一个长的非翻译区(426个核苷酸)。该片段富含G/C(68.5%),与开放阅读框区域不同,在麻疹病毒的M基因序列中似乎最不保守。将PPRV M蛋白与该组中的其他病毒蛋白进行比较,证实了之前所指出的该蛋白序列具有高度保守性。该组内的同一性百分比范围为76.7%至86.9%,与海豚麻疹病毒基质蛋白的同一性最高。