MAX (gene)

The protein product of MAX contains the basic helix-loop-helix and leucine zipper motifs. It is therefore included in the bHLHZ family of transcription factors. It is able to form homodimers with other MAX proteins and heterodimers with other transcription factors, including Mad, Mxl1 and Myc. The homodimers and heterodimers compete for a common DNA target site (the E-box) in a gene promoter zone. Rearrangement of dimers (e.g., Mad:Max, Max:Myc) provides a system of transcriptional regulation with greater diversity of gene targets. Max must dimerise in order to be biologically active.^[7]

Transcriptionally active hetero- and homodimers involving Max can promote cell proliferation as well as apoptosis.^[8]

The protein product of Max has been shown to interact with:

• Myc,^{[9][10][11][12][13][14][15][16][17][18][19][20][21]}
• MNT,^[18]
• MSH2,^[13]
• MXD1,^{[15][17][19][22]}
• MXI1,^{[16][18][20][23]}
• MYCL1,^[14][20]
• N-Myc,^[14][20]
• SPAG9,^[15]
• TEAD1,^[24] and
• Transformation/transcription domain-associated protein.^[10][11]

This gene has been shown mutated in cases of hereditary pheochromocytoma.^[25] More recently the Max gene becomes mutated and becomes inactivated in small cell lung cancer (SCLC). This is mutually exclusive with alterations at Myc and BRG1, the latter coding for an ATPase of the SWI/SNF complex. It was demonstrated that the BRG1 product regulates the expression of Max through direct recruitment to the Max promoter region, and that depletion of BRG1 strongly hinders cell growth, specifically in Max-deficient cells, suggesting that the two together cause synthetic lethality. Furthermore, Max required BRG1 to activate neuroendocrine transcriptional programs and to up-regulate Myc targets, such as glycolytic-related genes.^[26]

• MAX+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
• FactorBook Max

This article incorporates text from the United States National Library of Medicine, which is in the public domain.