Carbohydrate-responsive element-binding protein

MLXIPL
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	4GNT
Identifiers
Aliases	MLXIPL, CHREBP, MIO, MONDOB, WBSCR14, WS-bHLH, bHLHd14, MLX interacting protein like, MLX
External IDs	MGI: 1927999 HomoloGene: 32507 GeneCards: MLXIPL
Gene location (Human)
Chr.	Chromosome 7 (human)[1]
End	73,624,543 bp[1]
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)[2]
End	135,138,382 bp[2]
RNA expression pattern
	More reference expression data
Gene ontology
Molecular function	• carbohydrate response element binding; • DNA binding; • protein dimerization activity; • protein homodimerization activity; • transcription factor activity, sequence-specific DNA binding; • transcription factor binding; • RNA polymerase II core promoter proximal region sequence-specific DNA binding; • transcriptional repressor activity, RNA polymerase II core promoter proximal region sequence-specific binding; • protein heterodimerization activity; • RNA polymerase II transcription factor activity, sequence-specific DNA binding;
Cellular component	• transcription factor complex; • nucleoplasm; • cell nucleus; • cytoplasm; • cytosol;
Biological process	• intracellular signal transduction; • positive regulation of lipid biosynthetic process; • regulation of transcription, DNA-templated; • glucose homeostasis; • regulation of transcription from RNA polymerase II promoter; • anatomical structure morphogenesis; • negative regulation of transcription from RNA polymerase II promoter; • positive regulation of fatty acid biosynthetic process; • transcription, DNA-templated; • negative regulation of cell cycle arrest; • positive regulation of transcription, DNA-templated; • fatty acid homeostasis; • positive regulation of cell proliferation; • negative regulation of peptidyl-serine phosphorylation; • glucose mediated signaling pathway; • negative regulation of oxidative phosphorylation; • negative regulation of transcription, DNA-templated; • positive regulation of glycolytic process; • triglyceride homeostasis; • positive regulation of transcription from RNA polymerase II promoter; • cellular response to carbohydrate stimulus; • energy homeostasis;
	Sources:Amigo / QuickGO
Orthologs
	51085
	58805
	ENSG00000009950
	ENSMUSG00000005373
	Q9NP71
	Q99MZ3
	NM_032951; NM_032952; NM_032953; NM_032954; NM_032994
	NM_021455; NM_001359237
	NP_116569; NP_116570; NP_116571; NP_116572
	NP_067430; NP_001346166
	Wikidata
View/Edit Human	View/Edit Mouse

Carbohydrate-responsive element-binding protein (ChREBP) also known as MLX-interacting protein-like (MLXIPL) is a protein that in humans is encoded by the MLXIPL gene.^[5]^[6] The protein name derives from the protein's interaction with carbohydrate response element sequences of DNA.

Function

This gene encodes a basic helix-loop-helix leucine zipper transcription factor of the Myc / Max / Mad superfamily. This protein forms a heterodimeric complex and binds and activates, in a glucose-dependent manner, carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes.^[6]

Clinical significance

This gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23.^[6]

Interactions

MLXIPL has been shown to interact with MLX.^[7]

Role in glycolysis

ChREBP is translocated to the nucleus and binds to DNA after dephosphorylation of a p-Ser and a p-Thr residue by PP2A, which itself is activated by Xylulose-5-phosphate. Xu5p is produced in the pentose phosphate pathway when levels of Glucose-6-phosphate are high (the cell has ample glucose). In the liver, ChREBP mediates activation of several regulatory enzymes of glycolysis and lipogenesis including L-type pyruvate kinase (L-PK), acetyl CoA carboxylase, and fatty acid synthase.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000009950 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000005373 - Ensembl, May 2017
↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ Meng X, Lu X, Li Z, Green ED, Massa H, Trask BJ, Morris CA, Keating MT (Jan 1999). "Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes". Hum Genet. 103 (5): 590–9. doi:10.1007/s004390050874. PMID 9860302.
1 2 3 "Entrez Gene: MLXIPL MLX interacting protein-like".
↑ Cairo S, Merla G, Urbinati F, Ballabio A, Reymond A (March 2001). "WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network". Hum. Mol. Genet. 10 (6): 617–27. doi:10.1093/hmg/10.6.617. PMID 11230181.

de Luis O, Valero MC, Jurado LA (2000). "WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog". Eur. J. Hum. Genet. 8 (3): 215–22. doi:10.1038/sj.ejhg.5200435. PMID 10780788.
Cairo S, Merla G, Urbinati F, et al. (2001). "WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network". Hum. Mol. Genet. 10 (6): 617–27. doi:10.1093/hmg/10.6.617. PMID 11230181.
Kawaguchi T, Takenoshita M, Kabashima T, Uyeda K (2002). "Glucose and cAMP regulate the L-type pyruvate kinase gene by phosphorylation/dephosphorylation of the carbohydrate response element binding protein". Proc. Natl. Acad. Sci. U.S.A. 98 (24): 13710–5. doi:10.1073/pnas.231370798. PMC 61106. PMID 11698644.
Kawaguchi T, Osatomi K, Yamashita H, et al. (2002). "Mechanism for fatty acid "sparing" effect on glucose-induced transcription: regulation of carbohydrate-responsive element-binding protein by AMP-activated protein kinase". J. Biol. Chem. 277 (6): 3829–35. doi:10.1074/jbc.M107895200. PMID 11724780.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Hillman RT, Green RE, Brenner SE (2005). "An unappreciated role for RNA surveillance". Genome Biol. 5 (2): R8. doi:10.1186/gb-2004-5-2-r8. PMC 395752. PMID 14759258.
Merla G, Howald C, Antonarakis SE, Reymond A (2005). "The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3". Hum. Mol. Genet. 13 (14): 1505–14. doi:10.1093/hmg/ddh163. PMID 15163635.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Li MV, Chang B, Imamura M, et al. (2006). "Glucose-dependent transcriptional regulation by an evolutionarily conserved glucose-sensing module". Diabetes. 55 (5): 1179–89. doi:10.2337/db05-0822. PMID 16644671.

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[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000009950 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000005373 - Ensembl, May 2017

[3] "Human PubMed Reference:".

[4] "Mouse PubMed Reference:".

[pmid9860302-5] Meng X, Lu X, Li Z, Green ED, Massa H, Trask BJ, Morris CA, Keating MT (Jan 1999). "Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes". Hum Genet. 103 (5): 590–9. doi:10.1007/s004390050874. PMID 9860302.

[entrez-6] 1 2 3 "Entrez Gene: MLXIPL MLX interacting protein-like".

[pmid11230181-7] Cairo S, Merla G, Urbinati F, Ballabio A, Reymond A (March 2001). "WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network". Hum. Mol. Genet. 10 (6): 617–27. doi:10.1093/hmg/10.6.617. PMID 11230181.