HLX (gene)

HLX
Identifiers
Aliases HLX, HB24, HLX1, H2.0 like homeobox
External IDs MGI: 96109 HomoloGene: 7363 GeneCards: HLX
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

3142

15284

Ensembl

ENSG00000136630

ENSMUSG00000039377

UniProt

Q14774

Q61670

RefSeq (mRNA)

NM_021958

NM_008250

RefSeq (protein)

NP_068777.1

NP_032276.1

Location (UCSC) Chr 1: 220.88 – 220.89 Mb Chr 1: 184.73 – 184.73 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

H2.0-like homeobox protein is a protein that in humans is encoded by the HLX gene.[3][4][5]

Role in development

Hlx belongs to the class of homeobox transcription factors, initially cloned from a B-lymphocyte cell line.[6] Targeted knockout of the gene has demonstrated its vital role in liver and gut organogenesis.[7] Its expression is first noticed in embryonic day 9.5 (E9.5) in the splanchnic mesoderm caudal to the level of the heart and foregut pocket, and in the branchial arches. Around E10- E12.5, the expression becomes more prominent in the mesenchyme of the visceral organs of the gut such as liver, intestines and gall bladder.[8] Hlx is essential for liver and gut expansion, but not for onset of their development. Heterozygous knockouts of Hlx (Hlx +/−) are normal whereas homozygous knockouts (Hlx −/–) develop severe hypoplasia of the liver and gut along with anaemia. Hlx controls the epithelial-mesenchymal interaction necessary for liver and gut expansion.[7] At E8.0, the primary liver bud is formed from the midgut endoderm in response to signals from the cardiogenic mesoderm. This is followed by signals from the septum transversum that induce epithelial-mesenchymal transition in the hepatic progenitors of the gut endoderm.[9][10] In a third stage, these signaling factors induce the liver endoderm to undergo proliferation and form liver cords. The same factor controls gut proliferation, and Hlx governs its expression. Although these mice develop anaemia, it is likely due to insufficient support from the liver in producing matrix component needed for hematopoiesis rather than an intrinsic defect in the hematopoietic cells.[7]

References

  1. ↑ "Human PubMed Reference:".
  2. ↑ "Mouse PubMed Reference:".
  3. ↑ Deguchi Y, Moroney JF, Wilson GL, Fox CH, Winter HS, Kehrl JH (April 1991). "Cloning of a human homeobox gene that resembles a diverged Drosophila homeobox gene and is expressed in activated lymphocytes". The New Biologist. 3 (4): 353–63. PMID 1676597.
  4. ↑ Kennedy MA, Rayner JC, Morris CM (July 1994). "Genomic structure, promoter sequence, and revised translation of human homeobox gene HLX1". Genomics. 22 (2): 348–55. doi:10.1006/geno.1994.1394. PMID 7806220.
  5. ↑ "Entrez Gene: HLX1 H2.0-like homeobox 1 (Drosophila)".
  6. ↑ Allen JD, Lints T, Jenkins NA, Copeland NG, Strasser A, Harvey RP, Adams JM (1991). "Novel murine homeo box gene on chromosome 1 expressed in specific hematopoietic lineages and during embryogenesis". Genes & Development. 5 (4): 509–20. doi:10.1101/gad.5.4.509. PMID 1672660.
  7. 1 2 3 Hentsch B, Lyons I, Li R, Hartley L, Lints TJ, Adams JM, Harvey RP (1996). "Hlx homeo box gene is essential for an inductive tissue interaction that drives expansion of embryonic liver and gut". Genes & Development. 10 (1): 70–9. doi:10.1101/gad.10.1.70. PMID 8557196.
  8. ↑ Lints TJ, Hartley L, Parsons LM, Harvey RP (1996). "Mesoderm-specific expression of the divergent homeobox gene Hlx during murine embryogenesis". Developmental Dynamics. 205 (4): 457–70. doi:10.1002/(SICI)1097-0177(199604)205:4<457::AID-AJA9>3.0.CO;2-H. PMID 8901056.
  9. ↑ Douarin NM (1975). "An experimental analysis of liver development". Medical Biology. 53 (6): 427–55. PMID 765644.
  10. ↑ Fukuda-Taira S (1981). "Hepatic induction in the avian embryo: specificity of reactive endoderm and inductive mesoderm". Journal of Embryology and Experimental Morphology. 63: 111–25. PMID 7310284.

Further reading

  • Najfeld V, Menninger J, Ballard SG, Deguchi Y, Ward DC, Kehrl JH (November 1992). "Two diverged human homeobox genes involved in the differentiation of human hematopoietic progenitors map to chromosome 1, bands q41-42.1". Genes, Chromosomes & Cancer. 5 (4): 343–7. doi:10.1002/gcc.2870050410. PMID 1283323. 
  • Deguchi Y, Thevenin C, Kehrl JH (April 1992). "Stable expression of HB24, a diverged human homeobox gene, in T lymphocytes induces genes involved in T cell activation and growth". The Journal of Biological Chemistry. 267 (12): 8222–9. PMID 1349016. 
  • Deguchi Y, Kirschenbaum A, Kehrl JH (June 1992). "A diverged homeobox gene is involved in the proliferation and lineage commitment of human hematopoietic progenitors and highly expressed in acute myelogenous leukemia". Blood. 79 (11): 2841–8. PMID 1375114. 
  • Allen JD, Lints T, Jenkins NA, Copeland NG, Strasser A, Harvey RP, Adams JM (April 1991). "Novel murine homeo box gene on chromosome 1 expressed in specific hematopoietic lineages and during embryogenesis". Genes & Development. 5 (4): 509–20. doi:10.1101/gad.5.4.509. PMID 1672660. 
  • Deguchi Y, Kehrl JH (July 1991). "Selective expression of two homeobox genes in CD34-positive cells from human bone marrow". Blood. 78 (2): 323–8. PMID 1712647. 
  • Deguchi Y, Yamanaka Y, Theodossiou C, Najfeld V, Kehrl JH (March 1993). "High expression of two diverged homeobox genes, HB24 and HB9, in acute leukemias: molecular markers of hematopoietic cell immaturity". Leukemia. 7 (3): 446–51. PMID 7680402. 
  • Deguchi Y, Agus D, Kehrl JH (February 1993). "A human homeobox gene, HB24, inhibits development of CD4+ T cells and impairs thymic involution in transgenic mice". The Journal of Biological Chemistry. 268 (5): 3646–53. PMID 8094082. 
  • Nishimura DY, Purchio AF, Murray JC (February 1993). "Linkage localization of TGFB2 and the human homeobox gene HLX1 to chromosome 1q". Genomics. 15 (2): 357–64. doi:10.1006/geno.1993.1068. PMID 8095486. 
  • Quinn LM, Johnson BV, Nicholl J, Sutherland GR, Kalionis B (March 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. doi:10.1016/S0378-1119(96)00706-8. PMID 9073066. 
  • Quinn LM, Kilpatrick LM, Latham SE, Kalionis B (May 1998). "Homeobox genes DLX4 and HB24 are expressed in regions of epithelial-mesenchymal cell interaction in the adult human endometrium". Molecular Human Reproduction. 4 (5): 497–501. doi:10.1093/molehr/4.5.497. PMID 9665637. 
  • Murthi P, Doherty V, Said J, Donath S, Brennecke SP, Kalionis B (February 2006). "Homeobox gene HLX1 expression is decreased in idiopathic human fetal growth restriction". The American Journal of Pathology. 168 (2): 511–8. doi:10.2353/ajpath.2006.050637. PMC 1606485Freely accessible. PMID 16436665. 
  • Becknell B, Hughes TL, Freud AG, Blaser BW, Yu J, Trotta R, Mao HC, Caligiuri de Jesús ML, Alghothani M, Benson DM, Lehman A, Jarjoura D, Perrotti D, Bates MD, Caligiuri MA (March 2007). "Hlx homeobox transcription factor negatively regulates interferon-gamma production in monokine-activated natural killer cells". Blood. 109 (6): 2481–7. doi:10.1182/blood-2006-10-050096. PMC 1852195Freely accessible. PMID 17110450. 

External links

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


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