Generation and characterization of APOBEC3G-positive 293T cells for HIV-1 Vif study.
نویسندگان
چکیده
We have established a number of 293T cell lines that express a human anti HIV-1 factor APOBEC3G. Out of seven cell clones examined, four were readily demonstrated to express APOBEC3G by immunoblotting analysis. In particular, two clones (A3G-C1 and -C4) were found to produce a much higher level of functional APOBEC3G relative to that by pooled cell clones. The transfection efficiency of all these cell clones were similar to that of the parental cells, producing a comparable level of virions upon transfection of wild type and vif-minus proviral DNA clones. Furthermore, the expression level of APOBEC3G in the best cell line (A3G-C1) was far much higher than those of an APOBEC3G-positive lymphocyte cell line and peripheral blood mononuclear cells. We finally monitored the incorporation of APOBEC3G into virions produced in A3G-C1. APOBEC3G was easily detected in progeny viral particles upon transfection of vif-minus proviral clone but not of wild type. These results indicated that our new A3G-C1 cell line is eminently useful for various studies on the interaction of human APOBEC3G and HIV-1 Vif.
منابع مشابه
تولید سلول های ناپذیرا برای مطالعه HIV-1 vif
سابقه و هدف: مولکول APOBEC3G ، به عنوان فاکتور سلولی دخیل در میانکنش با vif HIV-1 عمل میکند که برای بررسی میانکنش آن با vif HIV-1 ، از سلولهای ناپذیرای طبیعی و ذاتی مثل H9 و PBMC انسانی مولد APOBEC3G استفاده میشود. به دلیل ناکارآمدی آنها در این نوع بررسیها، نیازمند سلولهای ناپذیرایی بودیم که به طور ثابت و به میزان بالا تولید APOBEC3G بنماید. لذا از سلولهای 293T برای ایجاد این دسته از سلول...
متن کاملVpr14-88-Apobec3G Fusion Protein Is Efficiently Incorporated into Vif-Positive HIV-1 Particles and Inhibits Viral Infection
BACKGROUND APOBEC3G (A3G), a deoxycytidine deaminase, is a potent host antiviral factor that can restrict HIV-1 infection. During Vif-negative HIV-1 replication, A3G is incorporated into HIV-1 particles, induces mutations in reverse transcribed viral DNA and inhibits reverse transcription. However, HIV-1 Vif counteracts A3G's activities by inducing its degradation and by blocking its incorporat...
متن کاملPolyubiquitination of APOBEC3G is essential for its degradation by HIV-1 Vif.
Proteasomal degradation of APOBEC3G is a critical step for human immunodeficiency virus type 1 (HIV-1) replication. However, the necessity for polyubiquitination of APOBEC3G in this process is still controversial. In this study, we showed that although macaque simian immunodeficiency virus (SIVmac) Vif is more stable than HIV-1 Vif in human cells, SIVmac Vif induces degradation of APBOEC3G as e...
متن کاملGenetic and functional characterization of HIV-1 Vif on APOBEC3G degradation: First report of emergence of B/C recombinants from North India
UNLABELLED HIV-1 is characterized by high genetic heterogeneity which is a challenge for developing therapeutics. Therefore, it is necessary to understand the extent of genetic variations that HIV is undergoing in North India. The objective of this study was to determine the role of genetic and functional role of Vif on APOBEC3G degradation. Vif is an accessory protein involved in counteracting...
متن کاملHIV-1 subtype variability in Vif derived from molecular clones affects APOBEC3G-mediated host restriction.
BACKGROUND The host protein APOBEC3G (A3G) can limit HIV-1 replication. Its protective effect is overcome by the HIV-1 'viral infectivity factor' (Vif), which targets A3G for proteosomal degradation. Although Vif is considered to be essential for HIV-1 replication, the effect of Vif variability among commonly used HIV-1 molecular clones of different genetic backgrounds on viral infectiousness a...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- The journal of medical investigation : JMI
دوره 54 1-2 شماره
صفحات -
تاریخ انتشار 2007