BASIC-HELIX-LOOP-HELIX

bHLH structural motif of the AhR protein: two α helices (blue) connected by a loop (red)

A 'basic-helix-loop-helix (bHLH)' is a protein structural motif that characterizes a family of transcription factors.

Contents
Structure
Examples
Regulation
History
References
External links

Structure


The motif is characterized by two α helices connected by a loop. Transcription factors including this domain are typically dimeric, each with one helix containing basic amino acid residues that facilitate DNA binding.[1] One helix is typically smaller and due to the flexibility of the loop, allows dimerization by folding and packing against another helix. The larger helix typically contains the DNA binding regions. bHLH proteins typically bind to a consensus sequence called an E-box, CANNTG. The canonical E-box is CACGTG (palindromic), however some bHLH transcription factors bind to different sequences, which are often similar to the E-box.

Examples


Examples of transcription factors containing a bHLH include:

AhR

BMAL-1-CLOCK

c-Myc

MyoD

HIF

NPAS1, MOP5

Scl, also known as Tal1

★ proneural bHLH genes like p-CaMKII, and pSer(336)NeuroD.
bHLH transcription factors are often important in development or cell activity. BMAL1-Clock is a core transcription complex in the molecular circadian clock. Other genes, like c-Myc and HIF-1 have been linked to cancer due to their effects on cell growth and metabolism.

Regulation


Since many bHLH transcription factors are heterodimeric, their activity is often highly regulated by the dimerization of the subunits. One subunit's expression or availability is often controlled while the other subunit is constituitively expressed. Many of the known regulatory proteins, such as the ''Drosophila'' extramacrochaetae protein, have the helix-loop-helix structure but lack the basic region, making them unable to bind to DNA on their own. They are, however, able to form heterodimers with proteins that have the bHLH structure and inactivate their abilities as transcription factors.[2]

History



★ 1989: Murre et al. could show that dimers of various bHLH proteins bind to a short DNA motif (later called E-Box).[3] This E-box consists of the DNA sequence CANNTG, where N can be any nucleotide.[4]

References


1. Molecular Cell Biology 5e + Cd-rom + Working With Molecular Cell Biology, Lodish, Harvey F., , , W H Freeman & Co (Sd), 2004,
2. Regulation of scute function by extramacrochaetae in vitro and in vivo, , Carlos V., Cabrera, Development, 1994
3. Interactions between heterologous helix-loop-helix proteins generate complexes that bind specifically to a common DNA sequence, Murre C, McCaw PS, Vaessin H, ''et al'', , , Cell, 1989
4. Basic Helix-Loop-Helix Proteins Can Act at the E-Box within the Serum Response Element of the c-fos Promoter to Influence Hormone-Induced Promoter Activation in Sertoli Cells, , Jaideep, Chaudhary, Molecular Endocrinology,

External links





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