Open Access Articles- Top Results for Msh homeobox 2

Msh homeobox 2

SymbolsMSX2 ; CRS2; FPP; HOX8; MSH; PFM; PFM1
External IDsOMIM123101 MGI97169 HomoloGene1837 GeneCards: MSX2 Gene
RNA expression pattern
File:PBB GE MSX2 205555 s at tn.png
File:PBB GE MSX2 210319 x at tn.png
More reference expression data
RefSeq (mRNA)NM_002449NM_013601
RefSeq (protein)NP_002440NP_038629
Location (UCSC)Chr 5:
174.15 – 174.16 Mb
Chr 13:
53.47 – 53.47 Mb
PubMed search[1][2]

Homeobox protein MSX-2 is a protein that in humans is encoded by the MSX2 gene.[1][2][3]

This gene encodes a member of the muscle segment homeobox gene family. The encoded protein is a transcriptional repressor whose normal activity may establish a balance between survival and apoptosis of neural crest-derived cells required for proper craniofacial morphogenesis. The encoded protein may also have a role in promoting cell growth under certain conditions and may be an important target for the RAS signaling pathways. Mutations in this gene are associated with parietal foramina 1 and craniosynostosis type 2.[3]


Msh homeobox 2 has been shown to interact with DLX5,[4] DLX2[4] and MSX1.[4]


  1. ^ Takahashi C, Akiyama N, Matsuzaki T, Takai S, Kitayama H, Noda M (Aug 1996). "Characterization of a human MSX-2 cDNA and its fragment isolated as a transformation suppressor gene against v-Ki-ras oncogene". Oncogene 12 (10): 2137–46. PMID 8668339. 
  2. ^ Kostrzewa M, Grady DL, Moyzis RK, Floter L, Muller U (Sep 1996). "Integration of four genes, a pseudogene, thirty-one STSs, and a highly polymorphic STRP into the 7-10 Mb YAC contig of 5q34-q35". Hum Genet 97 (3): 399–403. PMID 8786091. doi:10.1007/BF02185781. 
  3. ^ a b "Entrez Gene: MSX2 msh homeobox 2". 
  4. ^ a b c Zhang, H; Hu G; Wang H; Sciavolino P; Iler N; Shen M M; Abate-Shen C (May 1997). "Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism". Mol. Cell. Biol. (UNITED STATES) 17 (5): 2920–32. ISSN 0270-7306. PMC 232144. PMID 9111364. 

Further reading

  • Suzuki M, Tanaka M, Iwase T et al. (1993). "Over-expression of HOX-8, the human homologue of the mouse Hox-8 homeobox gene, in human tumors.". Biochem. Biophys. Res. Commun. 194 (1): 187–93. PMID 7687426. doi:10.1006/bbrc.1993.1802. 
  • Semenza GL, Wang GL, Kundu R (1995). "DNA binding and transcriptional properties of wild-type and mutant forms of the homeodomain protein Msx2.". Biochem. Biophys. Res. Commun. 209 (1): 257–62. PMID 7726844. doi:10.1006/bbrc.1995.1497. 
  • Iimura T (1995). "[Molecular cloning and expression of homeobox-containing genes during hard tissue development]". Kokubyo Gakkai Zasshi 61 (4): 590–604. PMID 7897272. doi:10.5357/koubyou.61.590. 
  • Hodgkinson JE, Davidson CL, Beresford J, Sharpe PT (1993). "Expression of a human homeobox-containing gene is regulated by 1,25(OH)2D3 in bone cells.". Biochim. Biophys. Acta 1174 (1): 11–6. PMID 8101453. doi:10.1016/0167-4781(93)90086-s. 
  • Jabs EW, Müller U, Li X et al. (1993). "A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis.". Cell 75 (3): 443–50. PMID 8106171. doi:10.1016/0092-8674(93)90379-5. 
  • Ma L, Golden S, Wu L, Maxson R (1997). "The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences.". Hum. Mol. Genet. 5 (12): 1915–20. PMID 8968743. doi:10.1093/hmg/5.12.1915. 
  • Quinn LM, Johnson BV, Nicholl J et al. (1997). "Isolation and identification of homeobox genes from the human placenta including a novel member of the Distal-less family, DLX4.". Gene 187 (1): 55–61. PMID 9073066. doi:10.1016/S0378-1119(96)00706-8. 
  • Zhang H, Hu G, Wang H et al. (1997). "Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism.". Mol. Cell. Biol. 17 (5): 2920–32. PMC 232144. PMID 9111364. 
  • Wu L, Wu H, Ma L et al. (1997). "Miz1, a novel zinc finger transcription factor that interacts with Msx2 and enhances its affinity for DNA.". Mech. Dev. 65 (1-2): 3–17. PMID 9256341. doi:10.1016/S0925-4773(97)00032-4. 
  • Newberry EP, Latifi T, Battaile JT, Towler DA (1997). "Structure-function analysis of Msx2-mediated transcriptional suppression.". Biochemistry 36 (34): 10451–62. PMID 9265625. doi:10.1021/bi971008x. 
  • Stelnicki EJ, Kömüves LG, Holmes D et al. (1997). "The human homeobox genes MSX-1, MSX-2, and MOX-1 are differentially expressed in the dermis and epidermis in fetal and adult skin.". Differentiation 62 (1): 33–41. PMID 9373945. doi:10.1046/j.1432-0436.1997.6210033.x. 
  • Iimura T, Takeda K, Goseki M et al. (1998). "Characterization of two length cDNA for human MSX-2 from dental pulp-derived cells.". DNA Seq. 8 (1-2): 87–92. PMID 9522127. doi:10.3109/10425179709020891. 
  • Newberry EP, Latifi T, Towler DA (1999). "The RRM domain of MINT, a novel Msx2 binding protein, recognizes and regulates the rat osteocalcin promoter.". Biochemistry 38 (33): 10678–90. PMID 10451362. doi:10.1021/bi990967j. 
  • Wilkie AO, Tang Z, Elanko N et al. (2000). "Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.". Nat. Genet. 24 (4): 387–90. PMID 10742103. doi:10.1038/74224. 
  • Wuyts W, Reardon W, Preis S et al. (2000). "Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.". Hum. Mol. Genet. 9 (8): 1251–5. PMID 10767351. doi:10.1093/hmg/9.8.1251. 
  • Quinn LM, Latham SE, Kalionis B (2000). "The homeobox genes MSX2 and MOX2 are candidates for regulating epithelial-mesenchymal cell interactions in the human placenta.". Placenta 21 (Suppl A): S50–4. PMID 10831122. doi:10.1053/plac.1999.0514. 
  • Masuda Y, Sasaki A, Shibuya H et al. (2001). "Dlxin-1, a novel protein that binds Dlx5 and regulates its transcriptional function.". J. Biol. Chem. 276 (7): 5331–8. PMID 11084035. doi:10.1074/jbc.M008590200. 
  • Shirakabe K, Terasawa K, Miyama K et al. (2002). "Regulation of the activity of the transcription factor Runx2 by two homeobox proteins, Msx2 and Dlx5.". Genes Cells 6 (10): 851–6. PMID 11683913. doi:10.1046/j.1365-2443.2001.00466.x. 

External links

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

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