TY - JOUR
T1 - The Tat protein of equine infectious anemia virus (EIAV) activates cellular gene expression by read-through transcription
AU - Rosin-Arbesfeld, Rina
AU - Willbold, Dieter
AU - Yaniv, Abraham
AU - Gazit, Arnona
N1 - Funding Information:
This research was supported by a Grant from the German–Israeli Foundation for Scientific Research and Development (G.I.F.).
PY - 1998/9/28
Y1 - 1998/9/28
N2 - The Tat protein of equine infectious anemia virus, EIAV, was shown to augment viral gene expression, presumably through interaction with the Tat responsive element, TAR. Recently, cell-free polyadenylation assays suggested that perturbation of the EIAV TAR secondary structure diminished polyadenylation efficiency. The present study indicates that the EIAV TAR regulates the efficiency of the 3'-end processing of viral RNA also in transfected cells. Moreover, our data suggest that the provision of the EIAV Tat protein in trans potentiates read-through transcription through the 3' viral long terminal repeat (3' LTR), thus suggesting activation of downstream-located cellular genes.
AB - The Tat protein of equine infectious anemia virus, EIAV, was shown to augment viral gene expression, presumably through interaction with the Tat responsive element, TAR. Recently, cell-free polyadenylation assays suggested that perturbation of the EIAV TAR secondary structure diminished polyadenylation efficiency. The present study indicates that the EIAV TAR regulates the efficiency of the 3'-end processing of viral RNA also in transfected cells. Moreover, our data suggest that the provision of the EIAV Tat protein in trans potentiates read-through transcription through the 3' viral long terminal repeat (3' LTR), thus suggesting activation of downstream-located cellular genes.
KW - Lentiviruses
KW - Polyadenylation
KW - TAR
UR - http://www.scopus.com/inward/record.url?scp=0032575915&partnerID=8YFLogxK
U2 - 10.1016/S0378-1119(98)00389-8
DO - 10.1016/S0378-1119(98)00389-8
M3 - Article
C2 - 9756988
AN - SCOPUS:0032575915
SN - 0378-1119
VL - 219
SP - 25
EP - 35
JO - Gene
JF - Gene
IS - 1-2
ER -