Tat (HIV)

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Tat (HIV)[edit | edit source]

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[edit | edit source]

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 | edit source]

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 | edit source]

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 | edit source]

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 | edit source]

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.

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Contributors: Prab R. Tumpati, MD