An E-box (enhancer box) is a DNA response element found in some eukaryotes that acts as a protein -binding site and has been found to regulate gene expression in neurons , muscles , and other tissues. Its specific DNA sequence, CANNTG (where N can be any nucleotide ), with a palindromic canonical sequence of CACGTG, is recognized and bound by transcription factors to initiate gene transcription . Once the transcription factors bind to the promoters through the E-box, other enzymes can bind to the promoter and facilitate transcription from DNA to mRNA .
35-562: The E-box was discovered in a collaboration between Susumu Tonegawa 's and Walter Gilbert 's laboratories in 1985 as a control element in immunoglobulin heavy-chain enhancer. They found that a region of 140 base pairs in the tissue-specific transcriptional enhancer element was sufficient for different levels of transcription enhancement in different tissues and sequences. They suggested that proteins made by specific tissues acted on these enhancers to activate sets of genes during cell differentiation. In 1989, David Baltimore's lab discovered
70-748: A basic region, which helps mediate recognition between the bHLH monomer and the E-box (the basic region interacts with the major groove of the DNA ). Depending on the DNA motif ("CAGCTG" versus "CACGTG") the bHLH protein has a different set of basic residues. The E-box binding is modulated by Zn in mice. The CT-Rich Regions (CTRR) located about 23 nucleotides upstream of the E-box is important in E-box binding, transactivation (increased rate of genetic expression), and transcription of circadian genes BMAL1 / NPAS2 and BMAL1/ CLOCK complexes. The binding specificity of different E-boxes
105-412: A gene that codes for a transcription factor Myc , is important in regulating mammalian cell proliferation and apoptosis . In 1991, researchers tested whether c-Myc could bind to DNA by dimerizing it to E12. Dimers of E6, the chimeric protein, were able to bind to an E-box element (GGCCACGTGACC) which was recognized by other HLH proteins. Expression of E6 suppressed the function of c-Myc, which showed
140-508: A link between the two. In 1996, it was found that Myc heterodimerizes with MAX and that this heterodimeric complex could bind to the CAC(G/A)TG E-box sequence and activate transcription. In 1998, it was concluded that the function of c-Myc depends upon activating transcription of particular genes through E-box elements. MyoD comes from the Mrf bHLH family and its main role is myogenesis ,
175-563: A professor at the Massachusetts Institute of Technology. In 1994, he was appointed as the first Director of the MIT Center for Learning and Memory, which developed under his guidance into The Picower Institute for Learning and Memory . Tonegawa resigned his directorship in 2006 and currently serves as a Picower Professor of Neuroscience and Biology and a Howard Hughes Medical Institute Investigator. Tonegawa also served as Director of
210-484: A target of the BMAL1/CLOCK complex. The E-box plays an important role in circadian genes; so far, nine E/E'BOX controlled circadian genes have been identified: PER1 , PER2, BHLHB2 , BHLHB3 , CRY1 , DBP , Nr1d1 , Nr1d2 , and RORC. As the E-box is connected to several circadian genes, it is possible that the genes and proteins associated with it are "crucial and vulnerable points in the (circadian) system." The E-box
245-557: Is a protein that in humans is encoded by the BHLHE40 gene . DEC1 encodes a basic helix-loop-helix protein expressed in various tissues. Expression in the chondrocytes is responsive to the addition of Bt2cAMP. Differentiated embryo chondrocyte expressed gene 1 is believed to be involved in the control of cell differentiation. This article incorporates text from the United States National Library of Medicine , which
280-509: Is found to be essential in their function. E-boxes with different functions have a different number and type of binding factor. The consensus sequence of the E-box is usually CANNTG; however, there exist other E-boxes of similar sequences called noncanonical E-boxes. These include, but are not limited to: The link between E-box-regulated genes and the circadian clock was discovered in 1997, when Hao, Allen, and Hardin (Department of Biology at Texas A&M University ) analyzed rhythmicity in
315-525: Is now a freelance science writer. The Tonegawas have three children, Hidde Tonegawa, Hanna Tonegawa, and Satto Tonegawa (deceased). Tonegawa is a fan of the Boston Red Sox, and threw out an opening pitch during their 2004 World Series championship season. BHLHB2 8553 20893 ENSG00000134107 ENSMUSG00000030103 O14503 O35185 NM_003670 NM_011498 NP_003661 NP_035628 Class E basic helix-loop-helix protein 40
350-586: Is one of the top five transcription factor families associated with the circadian phase and is found in most tissues. A total of 320 E-box-controlled genes are found in the SCN ( suprachiasmatic nucleus ), liver , aorta , adrenal , WAT ( white adipose tissue ), brain , atria , ventricle , prefrontal cortex , skeletal muscle , BAT ( brown adipose tissue ), and calvarial bone. E-box like CLOCK-related elements (EL-box; GGCACGAGGC) are also important in maintaining circadian rhythmicity in clock-controlled genes. Similarly to
385-470: Is produced by alternative spliced E2A in E47 specific bHLH-encoding exons . Its role is to regulate tissue specific gene expression and differentiation. Many kinases have been associated with E47 including 3pk and MK2. These 2 proteins form a complex with E47 and reduce its transcription activity. CKII and PKA are also shown to phosphorylate E47 in vitro. Similar to other E-box binding proteins, E47 also binds to
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#1733085276437420-533: Is surmised that specific bases are necessary to support this high affinity binding. Furthermore, the sequence constraints on the region around the circadian E-box are not fully understood: it is believed to be necessary but not sufficient for E-boxes to be randomly spaced from each other in the genetic sequence in order for circadian transcription to occur. Recent research involving the E-box has been aimed at trying to find more binding proteins as well as discovering more mechanisms for inhibiting binding. Researchers at
455-408: The DNA of B cells (a type of white blood cell ) in embryonic and adult mice , he observed that genes in the mature B cells of the adult mice are moved around, recombined, and deleted to form the diversity of the variable region of antibodies. This process is known as V(D)J recombination . In 1983, Tonegawa also discovered a transcriptional enhancer element associated with antibody gene complex,
490-564: The Nobel Prize for Physiology or Medicine in 1987 for his discovery of V(D)J recombination , the genetic mechanism which produces antibody diversity. Although he won the Nobel Prize for his work in immunology , Tonegawa is a molecular biologist by training and he again changed fields following his Nobel Prize win; he now studies neuroscience , examining the molecular, cellular and neuronal basis of memory formation and retrieval. Tonegawa
525-664: The RIKEN Brain Science Institute from 2009 to 2017. Tonegawa's Nobel Prize work elucidated the genetic mechanism of the adaptive immune system , which had been the central question of immunology for over 100 years. Prior to Tonegawa's discovery, one early idea to explain the adaptive immune system suggested that each gene produces one protein; however, there are under 19,000 genes in the human body which nonetheless can produce millions of antibodies. In experiments beginning in 1976, Tonegawa showed that genetic material rearranges itself to form millions of antibodies. Comparing
560-477: The circadian clock . E-box binding proteins play a major role in regulating transcriptional activity. These proteins usually contain the basic helix-loop-helix protein structural motif , which allows them to bind as dimers . This motif consists of two amphipathic α-helices , separated by a small sequence of amino acids , that form one or more β-turns. The hydrophobic interactions between these α-helices stabilize dimerization. Besides, each bHLH monomer has
595-616: The CANNTG sequence in the E-box. In homozygous E2A knock-out mice, B cells development stops before the DJ arrangement stage and the B cells fail to mature. E47 has been shown to bind either as heterodimer(with E12) or as homodimer(but weaker). Although the structural basis for how BMAL1/CLOCK interact with the E-box is unknown, recent research has shown that the bHLH protein domains of BMAL1/CLOCK are highly similar to other bHLH containing proteins, e.g. Myc/Max, which have been crystallized with E-boxes. It
630-569: The E-box and affect gene transcription. The CLOCK- ARNTL (BMAL1) complex is an integral part of the mammalian circadian cycle and vital in maintaining circadian rhythmicity. Knowing that binding activates transcription of the per gene in the promoter region, researchers discovered in 2002 that DEC1 and DEC2 (bHLH transcription factors) repressed the CLOCK-BMAL1 complex through direct interaction with BMAL1 and/or competition for E-box elements. They concluded that DEC1 and DEC2 were regulators of
665-403: The E-box itself. These nucleotides determine the 3-D spatial arrangement of the DNA strand and restrict the size of binding transcription factors . The study also found differences in binding patterns between in vivo and in vitro strands. Susumu Tonegawa Susumu Tonegawa ( 利根川 進 , Tonegawa Susumu , born September 5, 1939) is a Japanese scientist who was the sole recipient of
700-464: The E-box, the E-box like CLOCK related element can also induce transcription of BMAL1/CLOCK, which can then lead to expression in other EL-box containing genes (Ank, DBP, Nr1d1). However, there are differences between the EL-box and the regular E-box. Suppressing DEC1 and DEC2 has a stronger effect on E-box than on EL-box. Furthermore, HES1, which can bind to a different consensus sequence (CACNAG, known as
735-472: The E2-2 was discovered in 1997 and was found to inhibit the promoter of a muscle-specific gene. Since then, researchers have established that the E-box affects gene transcription in several eukaryotes and found E-box binding factors that identify E-box consensus sequences . In particular, several experiments have shown that the E-box is an integral part of the transcription-translation feedback loop that comprises
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#1733085276437770-522: The Medical School of Nanjing University found that the amplitude of FBXL3 (F-box/Leucine rich-repeat protein) is expressed via an E-box. They studied mice with FBXL3 deficiency and found that it regulates feedback loops in circadian rhythms by affecting circadian period length. A study published April 4, 2013 by researchers at Harvard Medical School found that the nucleotides on either side of an E-box influences which transcription factors can bind to
805-521: The MyoD transcription factor family. MyoG-E-Box binding is necessary for neuromuscular synapse formation as an HDAC-Dach2- myogenin signaling pathway in skeletal muscle gene expression has been identified. Decreased MyoG expression has been shown in patients with muscle wasting symptom. MyoG and MyoD have also been shown to involve in myoblast differentiation. They act by transactivating cathepsin B promotor activity and inducing its mRNA expression. E47
840-576: The N-box), shows suppression effect in EL-box, but not in E-box. Both non-canonical E-boxes and E-box-like sequences are crucial for circadian oscillation. Recent research on this forms an hypothesis that either a canonical or non-canonical E-box followed by an E-box like sequence with 6 base pair interval in between is a necessary combination for circadian transcription. In silico analysis also suggests that such an interval existed in other known clock-controlled genes. There are several proteins that bind to
875-499: The activation of a specific sub-population of mouse hippocampal neurons, labelled during a fear conditioning paradigm, is sufficient to evoke a behavioral response correlated with a precise memory trace. This demonstrated for the first time that memory information is stored in specific cellular ensembles in the hippocampus , now frequently called memory engram cells. More recently, his lab continues to employ optogenetic technology and virus injection techniques to expand their findings on
910-581: The engram cell ensemble. Notably, Tonegawa has uncovered the role of memory engram cell ensembles in memory valence, social memory, as well as their role in brain disorders such as depression, amnesia, and Alzheimer's disease. These works provide proofs of concept for future medical treatments in humans through the manipulation of memory engram ensembles. Tonegawa currently resides in the Boston area with his wife, Mayumi Yoshinari Tonegawa, who worked as an NHK (Japan Broadcasting Corporation) director/interviewer and
945-562: The first cellular enhancer element. Shortly following his Nobel Prize, Tonegawa again changed fields from immunology to neuroscience, where he has focused his research in the ensuing years. Tonegawa's lab pioneered introductory transgenic and gene-knockout technologies in mammalian systems. He was involved in early work demonstrating the importance of CaMKII- (1992) and the NMDA receptor-dependent synaptic plasticity (1996) in memory formation. Tonegawa's lab discovered that dendritic neuronal spines in
980-422: The first two E-box binding proteins , E12 and E47. These immunoglobulin enhancers could bind as heterodimers to proteins through bHLH domains. In 1990, another E-protein, ITF-2A (later renamed E2-2Alt) was discovered that can bind to immunoglobulin light chain enhancers. Two years later, the third E-box binding protein, HEB, was discovered by screening a cDNA library from HeLa cells. A splice-variant of
1015-417: The formation of muscular tissue. Other members in this family include myogenin , Myf5 , Myf6 , Mist1 , and Nex-1. When MyoD binds to the E-box motif CANNTG, muscle differentiation and expression of muscle-specific proteins is initiated. The researchers ablated various parts of the recombinant MyoD sequence and concluded that MyoD used encompassing elements to bind the E-box and the tetralplex structure of
1050-405: The mammalian molecular clock. In 2006, Ripperger and Schibler discovered that the binding of this complex to the E-box drove circadian DBP transcription and chromatin transitions (a change from chromatin to facultative heterochromatin ). It was concluded that CLOCK regulates DBP expression by binding to E-box motifs in enhancer regions located in the first and second introns . MYC ( c-Myc ),
1085-499: The period ( per ) gene in Drosophila melanogaster . They found a circadian transcriptional enhancer upstream of the per gene within a 69 bp DNA fragment. Depending upon PER protein levels, the enhancer drove high levels of mRNA transcription in both LD (light-dark) and DD (constant darkness) conditions. The enhancer was found to be necessary for high-level gene expression but not for circadian rhythmicity. It also works independently as
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1120-550: The promoter sequence of the muscle specific gene α7 integrin and sarcomeric sMtCK . MyoD regulates HB-EGF ( Heparin-binding EGF-like growth factor ), a member of the EGF ( Epidermal growth factor ) family that stimulates cell growth and proliferation. It plays a role in the development of hepatocellular carcinoma , prostate cancer , breast cancer , esophageal cancer , and gastric cancer . MyoD can also bind to noncanonical E boxes of MyoG and regulate its expression. MyoG belongs to
1155-413: The temporal cortex are a likely target for treatment of Fragile X Syndrome. With one dosage of the inhibitor drug FRAX586, Tonegawa showed a marked reduction of FXS symptoms in the mouse model. Tonegawa was an early adopter of optogenetics and biotechnology in neuroscience research, leading to his groundbreaking work identifying and manipulating memory engram cells . In 2012, his lab demonstrated that
1190-795: The time, moved to the University of California, San Diego to do his doctorate study under Dr. Masaki Hayashi. He received his Ph.D. in 1968. Tonegawa conducted post-doctoral work at the Salk Institute in San Diego in the laboratory of Renato Dulbecco . With encouragement from Dr. Dulbecco, Tonegawa moved to the Basel Institute for Immunology in Basel, Switzerland in 1971, where he transitioned from molecular biology into immunology studies and carried out his landmark immunology studies. In 1981, Tonegawa became
1225-556: Was born in Nagoya , Japan and attended Hibiya High School in Tokyo. While a student at Kyoto University , Tonegawa became fascinated with operon theory after reading papers by François Jacob and Jacques Monod , whom he credits in part for inspiring his interest in molecular biology. Tonegawa graduated from Kyoto University in 1963 and, due to limited options for molecular biology study in Japan at
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