Howe Laboratory, Massachusetts Eye and Ear Infirmary, Department of Ophthalmology, Harvard Medical School, 243 Charles Street, Boston, MA 02114, USA.
Virus Res. 2011 Sep;160(1-2):120-7. doi: 10.1016/j.virusres.2011.05.022. Epub 2011 Jun 12.
Human adenovirus species D type 37 (HAdV-D37) is an important etiologic agent of epidemic keratoconjunctivitis. Annotation of the whole genome revealed an open reading frame (ORF) in the E3 transcription unit predicted to encode a 31.6kDa protein. This ORF, also known as CR1-γ, is predicted to be an integral membrane protein containing N-terminal signal sequence, luminal, transmembrane, and cytoplasmic domains. HAdV-D19 (C), another viral pathogen causing epidemic keratoconjunctivitis, contains an ORF 100% identical to its HAdV-D37 homologue but only 66% identical to other HAdV-D homologues. Kinetics of RNA expression and confirmation of splicing to the adenovirus tripartite leader sequence suggest a role for the protein product of CR1-γ in the late stages of the viral replication cycle. Confocal microscopy is consistent with expression in the cytoplasm. Sequence analysis reveals a hypervariable luminal domain and a conserved cytoplasmic domain. The luminal domain is predicted to contain multiple N-glycosylation sites. The cytoplasmic domain contains a putative protein kinase C phosphorylation site and potential YXXϕ and dileucine (LL) motifs suggesting a potential role in modification of host proteins.
人腺病毒 D 型 37 型(HAdV-D37)是流行角膜结膜炎的重要病原体。全基因组注释显示 E3 转录单元中的一个开放阅读框(ORF)预测编码一个 31.6kDa 的蛋白质。该 ORF 也称为 CR1-γ,预测为一种含有 N 端信号序列、腔、跨膜和细胞质结构域的完整膜蛋白。另一种引起流行角膜结膜炎的病毒病原体 HAdV-D19(C),其 ORF 与其 HAdV-D37 同源物 100%相同,但与其他 HAdV-D 同源物仅 66%相同。RNA 表达动力学和对腺病毒三分体前导序列的剪接证实表明,CR1-γ 蛋白产物在病毒复制周期的晚期起作用。共聚焦显微镜检查与细胞质中的表达一致。序列分析揭示了一个超变的腔结构域和一个保守的细胞质结构域。该腔结构域预测含有多个 N-糖基化位点。细胞质结构域包含一个假定的蛋白激酶 C 磷酸化位点和潜在的 YXXϕ 和亮氨酸(LL)基序,表明其在宿主蛋白修饰中可能发挥作用。