KMT2A: Difference between revisions
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= KMT2A = | |||
[[File:9aaTADs_in_the_E_protein_family.jpg|thumb|right|300px|Structure of 9aaTADs in the E protein family, relevant to KMT2A function.]] | |||
[[ | '''KMT2A''', also known as '''lysine methyltransferase 2A''', is a [[gene]] that encodes a protein involved in the regulation of [[gene expression]] through [[histone modification]]. This gene is located on [[chromosome 11]] in humans and is a member of the [[SET domain]] family of proteins, which are known for their role in [[epigenetic]] regulation. | ||
==Function== | == Function == | ||
KMT2A is a [[histone methyltransferase]] that specifically methylates [[histone H3]] at lysine 4 (H3K4). This modification is associated with [[transcriptional activation]] and is crucial for the regulation of [[gene expression]] during [[development]] and [[cell differentiation]]. The protein encoded by KMT2A contains several important domains, including a [[SET domain]], which is responsible for its methyltransferase activity, and [[PHD finger]] domains, which are involved in recognizing specific histone modifications. | |||
==Clinical | == Clinical significance == | ||
Mutations and | Mutations and rearrangements involving the KMT2A gene are implicated in various forms of [[leukemia]], particularly [[acute lymphoblastic leukemia]] (ALL) and [[acute myeloid leukemia]] (AML). These rearrangements often result in the formation of [[fusion proteins]] that disrupt normal gene regulation and contribute to the development of cancer. | ||
== | == Structure == | ||
[[File:Piskacek_Figures_v9b.jpg|thumb|left|300px|Diagram illustrating the structural domains of KMT2A.]] | |||
The KMT2A protein is a large, multi-domain protein that includes several [[zinc finger]] motifs, [[AT hooks]], and a [[SET domain]]. The presence of these domains allows KMT2A to interact with [[DNA]] and other [[chromatin]] components, facilitating its role in modifying chromatin structure and regulating gene expression. | |||
[[ | == Interactions == | ||
KMT2A interacts with a variety of other proteins to form a [[protein complex]] that is essential for its function in histone methylation. These interactions include binding with [[WDR5]], [[ASH2L]], and [[RBBP5]], which are components of the [[COMPASS complex]]. This complex is responsible for the trimethylation of H3K4, a key marker of active chromatin. | |||
== Related pages == | |||
==Related | |||
* [[Histone methylation]] | * [[Histone methylation]] | ||
* [[ | * [[Epigenetics]] | ||
* [[ | * [[Chromatin]] | ||
* [[ | * [[Leukemia]] | ||
* [[Gene expression | * [[Gene expression]] | ||
[[Category:Genes on human chromosome 11]] | [[Category:Genes on human chromosome 11]] | ||
[[Category:Epigenetics]] | |||
[[Category:Histone-modifying enzymes]] | [[Category:Histone-modifying enzymes]] | ||
Latest revision as of 14:11, 21 February 2025
KMT2A[edit]
KMT2A, also known as lysine methyltransferase 2A, is a gene that encodes a protein involved in the regulation of gene expression through histone modification. This gene is located on chromosome 11 in humans and is a member of the SET domain family of proteins, which are known for their role in epigenetic regulation.
Function[edit]
KMT2A is a histone methyltransferase that specifically methylates histone H3 at lysine 4 (H3K4). This modification is associated with transcriptional activation and is crucial for the regulation of gene expression during development and cell differentiation. The protein encoded by KMT2A contains several important domains, including a SET domain, which is responsible for its methyltransferase activity, and PHD finger domains, which are involved in recognizing specific histone modifications.
Clinical significance[edit]
Mutations and rearrangements involving the KMT2A gene are implicated in various forms of leukemia, particularly acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML). These rearrangements often result in the formation of fusion proteins that disrupt normal gene regulation and contribute to the development of cancer.
Structure[edit]
The KMT2A protein is a large, multi-domain protein that includes several zinc finger motifs, AT hooks, and a SET domain. The presence of these domains allows KMT2A to interact with DNA and other chromatin components, facilitating its role in modifying chromatin structure and regulating gene expression.
Interactions[edit]
KMT2A interacts with a variety of other proteins to form a protein complex that is essential for its function in histone methylation. These interactions include binding with WDR5, ASH2L, and RBBP5, which are components of the COMPASS complex. This complex is responsible for the trimethylation of H3K4, a key marker of active chromatin.
