LHX1

LHX1
Identifiers
Aliases LHX1, LIM-1, LIM1, LIM homeobox 1
External IDs MGI: 99783 HomoloGene: 4068 GeneCards: LHX1
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

3975

16869

Ensembl

n/a

ENSMUSG00000018698

UniProt

P48742
Q58F18

P63006

RefSeq (mRNA)

NM_005568

NM_008498

RefSeq (protein)

NP_005559.2
NP_005559.2

NP_032524.1

Location (UCSC) Chr 17: 36.94 – 36.94 Mb Chr 11: 84.52 – 84.53 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

LIM homeobox 1 is a protein that in humans is encoded by the LHX1 gene.[3]

This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor important for control of differentiation and development of neural and lymphoid cells. It is also key in development of renal and urogenital systems and is required for normal organogenesis.[4] A similar protein in mice is an essential regulator of the vertebrate head organizer.[3]

Function

The Lim gene family is a subfamily of homeobox genes.[5] The homeobox genes are essential in organizing the body plan of an organism and all contain the same conserved homeodomain of amino acids.[6] Evidence that Lim-1 is essential to a developing organism is its conservation throughout evolution and presence in a variety of organisms.[5] The Lim-1 gene encodes a transcription factor which binds to the DNA of specific genes and functions to produce the needed gene product for development of the organism.[7] Lim-1 is important during early molecular development and is required in both primitive streak-derived tissue and visceral endoderm of the early embryo for development of a head.[8] Studies done using mutant organisms without the Lim gene results in organisms that develop no head structure at all support the essential role of the Lim-1 gene in formation of the head.[9] This gene has also been shown to play a crucial role in the formation of the female reproductive tract.[7] The gene is expressed in the developing Müllerian duct of females, and when the gene is knocked out no reproductive tract forms.[7] Recent studies have shown that Lim-1 mutations may be one cause of the Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.[10] MRKH is characterized by defective development, or absence, of the uterus and upper part of the vagina in women with normal ovaries and karyotype.[10]

Lim-1’s expression is controlled in part by the sonic hedgehog-Gli signaling pathway.[4] Recent studies in mice have shown that Lim-1 silencing halts tumor growth and impairs tumor cell movement via inhibition of protein expression involved in metastatic spread.[4] Therefore, in tumor cells Lim-1 acts as an oncogene.[4] Thus, targeting Lim-1 can be a potential cancer therapy. In addition, Lim-1 is important in rodent renal development.[11] Lim-1 deficiency results in development of multicystic kidney, whereas, its expression can contribute to pathogenesis of nephroblastomas.[11] Also, Lim-1 plays a role in embryonic retinal development.[12] Lim-1 expression affects differentiation and maintenance of horizontal cells located in the retinal, thus, it could serve as a marker in studies of horizontal cell specification.[12]

References

  1. ↑ "Human PubMed Reference:".
  2. ↑ "Mouse PubMed Reference:".
  3. 1 2 "Entrez Gene: LHX1 LIM homeobox 1".
  4. 1 2 3 4 Dormoy, V.; et al. (2011). "LIM-class homeobox gene Lim1, a novel oncogene in human renal cell carcinoma.". Oncogene. 30 (15): 1753–1763. doi:10.1038/onc.2010.557. PMID 21132009.
  5. 1 2 Hobert, Oliver; Heiner Westphal (February 2000). "Functions of LIM-homeobox genes". Trends in Genetics. 16 (2): 75–83. doi:10.1016/S0168-9525(99)01883-1. Retrieved 2012-03-29.
  6. ↑ Carlson BM (2009). Human Embryology and Developmental Biology. Philadelphia, PA: Mosby Elsevier. pp. 67–70. ISBN 978-0-323-05385-3.
  7. 1 2 3 Kobayashi A, Shawlot W, Kania A, Behringer RR (Feb 2004). "Requirement of Lim1 for female reproductive tract development". Development. 131 (3): 539–49. doi:10.1242/dev.00951. PMID 14695376.
  8. ↑ Shawlot W, Wakamiya M, Kwan KM, Kania A, Jessell TM, Behringer RR (Nov 1999). "Lim1 is required in both primitive streak-derived tissues and visceral endoderm for head formation in the mouse" (PDF). Development. 126 (22): 4925–32. PMID 10529411.
  9. ↑ Bally-Cuif L, Boncinelli E (Feb 1997). "Transcription factors and head formation in vertebrates". BioEssays. 19 (2): 127–35. doi:10.1002/bies.950190207. PMID 9046242.
  10. 1 2 Ledig S, Brucker S, Barresi G, Schomburg J, Rall K, Wieacker P (Sep 2012). "Frame shift mutation of LHX1 is associated with Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome". Human Reproduction. 27 (9): 2872–5. doi:10.1093/humrep/des206. PMID 22740494.
  11. 1 2 Guertl B, Senanayake U, Nusshold E, Leuschner I, Mannweiler S, Ebner B, Hoefler G (2011). "Lim1, an embryonal transcription factor, is absent in multicystic renal dysplasia, but reactivated in nephroblastomas". Pathobiology. 78 (4): 210–9. doi:10.1159/000326769. PMID 21778788.
  12. 1 2 Liu W, Wang JH, Xiang M (Mar 2000). "Specific expression of the LIM/homeodomain protein Lim-1 in horizontal cells during retinogenesis". Developmental Dynamics. 217 (3): 320–5. doi:10.1002/(SICI)1097-0177(200003)217:3<320::AID-DVDY10>3.0.CO;2-F. PMID 10741426.

Further reading

  • Shawlot W, Behringer RR (Mar 1995). "Requirement for Lim1 in head-organizer function". Nature. 374 (6521): 425–30. doi:10.1038/374425a0. PMID 7700351. 
  • Bozzi F, Bertuzzi S, Strina D, Giannetto C, Vezzoni P, Villa A (Dec 1996). "The exon-intron structure of human LHX1 gene". Biochemical and Biophysical Research Communications. 229 (2): 494–7. doi:10.1006/bbrc.1996.1832. PMID 8954926. 
  • Dong WF, Heng HH, Lowsky R, Xu Y, DeCoteau JF, Shi XM, Tsui LC, Minden MD (Jun 1997). "Cloning, expression, and chromosomal localization to 11p12-13 of a human LIM/HOMEOBOX gene, hLim-1". DNA and Cell Biology. 16 (6): 671–8. doi:10.1089/dna.1997.16.671. PMID 9212161. 
  • Jurata LW, Pfaff SL, Gill GN (Feb 1998). "The nuclear LIM domain interactor NLI mediates homo- and heterodimerization of LIM domain transcription factors". The Journal of Biological Chemistry. 273 (6): 3152–7. doi:10.1074/jbc.273.6.3152. PMID 9452425. 
  • Ostendorff HP, Peirano RI, Peters MA, Schlüter A, Bossenz M, Scheffner M, Bach I (Mar 2002). "Ubiquitination-dependent cofactor exchange on LIM homeodomain transcription factors". Nature. 416 (6876): 99–103. doi:10.1038/416099a. PMID 11882901. 
  • Phillips JC (2003). "Assignment of LHX1 to human chromosome bands 17q11.2-->q12 by use of radiation hybrid mapping and somatic cell hybridization". Cytogenetic and Genome Research. 97 (1-2): 140D. doi:10.1159/000064048. PMID 12438757. 
This article is issued from Wikipedia - version of the 11/8/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.