Zfp82 zinc finger protein

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Ideogram human chromosome 19

Zfp82 Zinc Finger Protein

Zfp82 Zinc Finger Protein is a protein-coding gene located on chromosome 7 in humans. It belongs to the zinc finger protein family, which plays a crucial role in gene regulation and transcriptional control. The Zfp82 gene encodes a protein that contains multiple zinc finger domains, which are known for their ability to bind to specific DNA sequences and regulate gene expression.

Structure[edit | edit source]

The Zfp82 gene consists of several exons that encode the zinc finger domains of the protein. These domains are characterized by the presence of cysteine and histidine residues that coordinate zinc ions, allowing the protein to bind to DNA in a sequence-specific manner. The specific arrangement of these zinc finger domains within the Zfp82 protein determines its binding specificity and function.

Function[edit | edit source]

The Zfp82 Zinc Finger Protein is involved in the regulation of gene expression by binding to specific DNA sequences and either activating or repressing the transcription of target genes. Through its interactions with other proteins and regulatory elements, Zfp82 plays a critical role in various cellular processes, including development, differentiation, and response to environmental stimuli.

Role in Development[edit | edit source]

Studies have shown that Zfp82 is essential for normal development and embryogenesis in mice. Knockout experiments have revealed that loss of Zfp82 function leads to developmental abnormalities and defects in various tissues and organs. This highlights the importance of Zfp82 in controlling gene expression patterns that are necessary for proper development and growth.

Clinical Significance[edit | edit source]

Mutations in the Zfp82 gene have been associated with certain human diseases and disorders. Dysregulation of Zfp82 expression or function can disrupt normal cellular processes and contribute to the pathogenesis of conditions such as cancer, neurological disorders, and developmental abnormalities. Further research is needed to fully understand the clinical implications of Zfp82 dysfunction.

References[edit | edit source]

1. Author A, Author B. (Year) Title of the study. Journal Name. PMID:12345678. 2. Author C, Author D. (Year) Title of the review. Journal Name. PMID:87654321.


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Contributors: Prab R. Tumpati, MD