Ponti Donatella, Troiano Maria, Bellenchi Gian Carlo, Battaglia Piero A, Gigliani Franca
Dipartimento di Biotecnologie Cellulari ed Ematologia, Università La Sapienza, Roma, Italia.
BMC Cell Biol. 2008 Jun 17;9:32. doi: 10.1186/1471-2121-9-32.
Inside the cell, the HIV Tat protein is mainly found in the nucleus and nucleolus. The nucleolus, the site of ribosome biogenesis, is a highly organized, non-membrane-bound sub-compartment where proteins with a high affinity for nucleolar components are found. While it is well known that Tat accumulates in the nucleolus via a specific nucleolar targeting sequence, its function in this compartment it still unknown.
To clarify the significance of the Tat nucleolar localization, we induced the expression of the protein during oogenesis in Drosophila melanogaster strain transgenic for HIV-tat gene. Here we show that Tat localizes in the nucleoli of Drosophila oocyte nurse cells, where it specifically co-localizes with fibrillarin. Tat expression is accompanied by a significant decrease of cytoplasmic ribosomes, which is apparently related to an impairment of ribosomal rRNA precursor processing. Such an event is accounted for by the interaction of Tat with fibrillarin and U3 snoRNA, which are both required for pre-rRNA maturation.
Our data contribute to understanding the function of Tat in the nucleolus, where ribosomal RNA synthesis and cell cycle control take place. The impairment of nucleolar pre-rRNA maturation through the interaction of Tat with fibrillarin-U3snoRNA complex suggests a process by which the virus modulates host response, thus contributing to apoptosis and protein shut-off in HIV-uninfected cells.
在细胞内,HIV反式激活因子(Tat)蛋白主要存在于细胞核和核仁中。核仁是核糖体生物合成的场所,是一个高度有序、无膜包裹的亚结构,富含对核仁成分具有高亲和力的蛋白质。虽然已知Tat通过特定的核仁靶向序列在核仁中积累,但其在该亚结构中的功能仍不清楚。
为阐明Tat核仁定位的意义,我们在携带HIV-tat基因的转基因黑腹果蝇品系的卵子发生过程中诱导该蛋白的表达。我们在此表明,Tat定位于果蝇卵母细胞滋养细胞的核仁中,并与核仁纤维蛋白特异性共定位。Tat的表达伴随着细胞质核糖体的显著减少,这显然与核糖体rRNA前体加工受损有关。这种现象是由Tat与核仁纤维蛋白和U3小核仁RNA的相互作用引起的,这两者都是前体rRNA成熟所必需的。
我们的数据有助于理解Tat在核仁中的功能,核仁是核糖体RNA合成和细胞周期控制发生的场所。Tat与核仁纤维蛋白-U3小核仁RNA复合物相互作用导致核仁前体rRNA成熟受损,提示病毒调节宿主反应的一个过程,从而导致未感染HIV的细胞发生凋亡和蛋白质合成关闭。