Arya S K, Guo C, Josephs S F, Wong-Staal F
Science. 1985 Jul 5;229(4708):69-73. doi: 10.1126/science.2990040.
Human T-lymphotropic virus type III (HTLV-III) encodes a trans-acting factor that activates the expression of genes linked to the HTLV-III long terminal repeat. By functional mapping of complementary DNA transcripts of viral messenger RNA's the major functional domain of the gene encoding this factor was localized to a region immediately before the env gene of the virus, a region previously thought to be noncoding. This newly identified gene consists of three exons, and its transcription into messenger RNA involves two splicing events bringing together sequences from the 5' part (287 base pairs), middle (268 base pairs), and 3'part (1258 base pairs) of the HTLV-III genome. A similar messenger RNA with a truncated second exon (70 base pairs) does not encode a trans-acting function. It is proposed that this second messenger RNA is the transcript of a gene (3'-orf) located after the env gene. Messenger RNA's were also identified for the env and gag-pol genes of HTLV-III.
人类嗜T淋巴细胞病毒III型(HTLV-III)编码一种反式作用因子,该因子可激活与HTLV-III长末端重复序列相关的基因表达。通过对病毒信使RNA的互补DNA转录本进行功能定位,编码该因子的基因的主要功能域定位于病毒env基因之前紧邻的区域,该区域以前被认为是非编码区。这个新发现的基因由三个外显子组成,其转录成信使RNA涉及两次剪接事件,将HTLV-III基因组5'部分(287个碱基对)、中间部分(268个碱基对)和3'部分(1258个碱基对)的序列拼接在一起。一个具有截短的第二个外显子(70个碱基对)的类似信使RNA不编码反式作用功能。有人提出,这种第二个信使RNA是位于env基因之后的一个基因(3'-orf)的转录本。还鉴定出了HTLV-III的env和gag-pol基因的信使RNA。