Tat (HIV): Difference between revisions
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{{DISPLAYTITLE:Tat (HIV)}} | |||
The '''Tat''' | == Tat (HIV) == | ||
[[File:6CYT_HIV_Tat_TAR_complex.png|thumb|right|300px|Structure of the HIV Tat-TAR complex.]] | |||
The '''Tat protein''' is a crucial regulatory protein encoded by the [[Human Immunodeficiency Virus]] (HIV). It plays a significant role in the [[transcription]] of the viral genome, thereby enhancing the replication of the virus within the host cell. Tat stands for "Trans-Activator of Transcription." | |||
== Structure == | |||
Tat is a small protein, typically consisting of 86 to 101 amino acids, depending on the specific [[HIV subtype]]. The protein is characterized by several functional domains, including a [[cysteine]]-rich region, a basic domain, and a glutamine-rich region. These domains are essential for its interaction with the [[TAR RNA]] element and other cellular factors. | |||
== Function == | == Function == | ||
Tat is primarily involved in the transcriptional activation of the HIV [[long terminal repeat]] (LTR), which is the promoter region of the viral genome. It binds to the [[TAR RNA]] element, a stem-loop structure located at the 5' end of all nascent viral [[mRNA]] transcripts. This binding enhances the processivity of the [[RNA polymerase II]] enzyme, leading to increased transcription of the viral genome. | |||
== Mechanism of Action == | |||
Tat recruits several host cellular factors to the TAR RNA, including the [[positive transcription elongation factor b]] (P-TEFb), which consists of [[cyclin T1]] and [[CDK9]]. This recruitment leads to the phosphorylation of the C-terminal domain of RNA polymerase II, facilitating the transition from transcription initiation to elongation. | |||
== Role in HIV Pathogenesis == | == Role in HIV Pathogenesis == | ||
Tat is not only crucial for viral replication but also contributes to the pathogenesis of HIV. It has been shown to have [[neurotoxic]] effects, contributing to [[HIV-associated neurocognitive disorders]] (HAND). Additionally, Tat can modulate the expression of several host genes, influencing [[immune system]] function and contributing to the [[immune evasion]] strategies of the virus. | |||
== Therapeutic Target == | == Therapeutic Target == | ||
Given its essential role in HIV replication and pathogenesis, Tat is considered a potential target for [[antiretroviral therapy]]. Inhibitors of Tat function are being explored as therapeutic agents to suppress HIV replication and mitigate its pathogenic effects. | |||
== Related pages == | |||
* [[HIV structure and genome]] | |||
== | * [[HIV replication cycle]] | ||
* [[HIV/AIDS]] | |||
* [[HIV]] | * [[Antiretroviral drug]] | ||
* [[ | |||
* [[ | |||
* [[ | |||
[[Category:HIV]] | [[Category:HIV/AIDS]] | ||
[[Category:Viral proteins]] | [[Category:Viral proteins]] | ||
Latest revision as of 11:09, 15 February 2025
Tat (HIV)[edit]

The Tat protein is a crucial regulatory protein encoded by the Human Immunodeficiency Virus (HIV). It plays a significant role in the transcription of the viral genome, thereby enhancing the replication of the virus within the host cell. Tat stands for "Trans-Activator of Transcription."
Structure[edit]
Tat is a small protein, typically consisting of 86 to 101 amino acids, depending on the specific HIV subtype. The protein is characterized by several functional domains, including a cysteine-rich region, a basic domain, and a glutamine-rich region. These domains are essential for its interaction with the TAR RNA element and other cellular factors.
Function[edit]
Tat is primarily involved in the transcriptional activation of the HIV long terminal repeat (LTR), which is the promoter region of the viral genome. It binds to the TAR RNA element, a stem-loop structure located at the 5' end of all nascent viral mRNA transcripts. This binding enhances the processivity of the RNA polymerase II enzyme, leading to increased transcription of the viral genome.
Mechanism of Action[edit]
Tat recruits several host cellular factors to the TAR RNA, including the positive transcription elongation factor b (P-TEFb), which consists of cyclin T1 and CDK9. This recruitment leads to the phosphorylation of the C-terminal domain of RNA polymerase II, facilitating the transition from transcription initiation to elongation.
Role in HIV Pathogenesis[edit]
Tat is not only crucial for viral replication but also contributes to the pathogenesis of HIV. It has been shown to have neurotoxic effects, contributing to HIV-associated neurocognitive disorders (HAND). Additionally, Tat can modulate the expression of several host genes, influencing immune system function and contributing to the immune evasion strategies of the virus.
Therapeutic Target[edit]
Given its essential role in HIV replication and pathogenesis, Tat is considered a potential target for antiretroviral therapy. Inhibitors of Tat function are being explored as therapeutic agents to suppress HIV replication and mitigate its pathogenic effects.