Biology:LBH (gene)

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Short description: Protein-coding gene in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

The LBH (Limb Bud-Heart) gene is a highly conserved human gene that produces the LBH protein,[1] a transcription co-factor in the Wnt/β-catenin pathway.[2] Upon transcriptional activation of β-catenin, LBH goes on to act as a regulator of cell proliferation and differentiation through multiple transcriptional targets.[3][4] The gene is located on the p arm of chromosome 2 and is roughly 28 kb long.[1] Current ongoing studies are examining its role in developmental and oncological settings.

Gene

Located on chromosome 2, the full sequence is 28495 base pairs long. It contains three exons that will be translated to create the final protein product. Currently, there is no identified promoter region. LBH has a high degree of similarity among many vertebrate species.[1] This is most likely evident of its importance in development and stem cell regulation. Interestingly, LBH has no known paralogs, despite its multifunctionality and expression in different tissues at various stages of development.[1]

Protein

The LBH or Limb-Bud and Heart protein is 105 aa long nuclear protein and is highly conserved across vertebrate species.[1] LBH is a disordered, acidic protein. It lacks any globular fold or secondary and tertiary structures, placing it in the class of intrinsically disordered proteins (IDPs).[5] Research is ongoing on how LBHs conformational flexibility affects its role as a transcriptional regulator. IDPs are known to undergo disorder to order transitions in the presence of certain binding partners.[6] Due to LBHs disordered structure, it may experience multi-functionality through the binding to different targets, producing different transcriptional effects.

Mechanism

LBH or Limb-Bud-Heart was first identified in a 2001 study on transcriptional cofactors for limb patterning in mice. LBH was noted for its expression in developing limb buds and heart formation, hence its name. LBH was hypothesized to act as a transcriptional cofactor due to preliminary examinations of its protein structure and composition.[3] LBH was then found to be directly downstream of the canonical Wnt/β-catenin pathway by downregulating the expression of Wnt, preventing signal completion.[3] The Wnt/β-catenin pathway is a highly conserved pathway that is expressed in a variety of tissues and stages.[7] Direct overlap of in vivo expression of Wnt/β-catenin pathway activation and LBH expression during limb bud development gives evidence for a direct interaction between Wnt/β-catenin and LBH.[3]

Recent studies have found that LBH has a significant role in the regulation of stem cell growth and proliferation in mammary glands. LBH induces expression of ΔNp63, a key epithelial stem cell transcription factor, to promote basal MaSC differentiation and proliferation growing the basal mammary gland. This is compared to luminal expansion and differentiation, increasing the movement and differentiation of the basal MaSC cells to the luminal surface. Knockdowns in mice have resulted in reduced mammary gland growth during puberty and pregnancy.[4] Inversely, overexpression has been noted in basal subtype breast cancers, furthering LBHs effect on stem cell regulation.[3]

Diseases

The overexpression of LBH is one of the causal factors for birth defects seen in partial trisomy 2p syndrome, an autosomal disorder that causes multiple congenital defects. Partial trisomy 2p patients have a triplication of the p arm of chromosome 2.[8] Transgenic overexpression in mice of the LBH ortholog, Lbh, causes the continued overexpression and downregulation of multiple targets downstream of Lbh, mimicking symptoms of congenital heart disease (CHD) and skeletal defects seen in partial trisomy 2p patients. In addition to this, Lbh overexpression leads to the repression of Nkx2.5 and Tbx5, important regulators in cardiogenesis in developing embryos.[9] The importance of LBH in cardiogenesis is evident of LBHs multifunctionality despite being highly conserved and having no paralogs.

LBH also has an important oncological role in the development of mammary gland tumors. LBH has been noted for its overexpression in aggressive “basal” subtype breast cancers. Studies examining the role of Lbh in tumorigenesis in MMTV-Wnt1 transgenic mice as a model for Wnt induced breast cancer development. Lbh was conditionally deactivated in these transgenic mice, significantly delaying tumor onset and resulted in decreased differentiation and proliferation while also increasing apoptosis.[10]

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 "Genome Data Viewer - NCBI". https://www.ncbi.nlm.nih.gov/genome/gdv/browser/gene/?id=81606. 
  2. ↑ Briegel, Karoline J.; Joyner, Alexandra L. (2001-05-15). "Identification and Characterization of Lbh, a Novel Conserved Nuclear Protein Expressed during Early Limb and Heart Development" (in en). Developmental Biology 233 (2): 291–304. doi:10.1006/dbio.2001.0225. ISSN 0012-1606. PMID 11336496. 
  3. ↑ 3.0 3.1 3.2 3.3 3.4 Rieger, Megan E.; Sims, Andrew H.; Coats, Ebony R.; Clarke, Robert B.; Briegel, Karoline J. (September 2010). "The Embryonic Transcription Cofactor LBH Is a Direct Target of the Wnt Signaling Pathway in Epithelial Development and in Aggressive Basal Subtype Breast Cancers" (in en). Molecular and Cellular Biology 30 (17): 4267–4279. doi:10.1128/MCB.01418-09. ISSN 0270-7306. PMID 20606007. 
  4. ↑ 4.0 4.1 Lindley, Linsey E.; Curtis, Kevin M.; Sanchez-Mejias, Avencia; Rieger, Megan E.; Robbins, David J.; Briegel, Karoline J. (2015-03-01). "The WNT-controlled transcriptional regulator LBH is required for mammary stem cell expansion and maintenance of the basal lineage". Development 142 (5): 893–904. doi:10.1242/dev.110403. ISSN 0950-1991. PMID 25655704. PMC 4352974. https://doi.org/10.1242/dev.110403. 
  5. ↑ Al-Ali, Hassan; Rieger, Megan E.; Seldeen, Kenneth L.; Harris, Thomas K.; Farooq, Amjad; Briegel, Karoline J. (2010-01-01). "Biophysical characterization reveals structural disorder in the developmental transcriptional regulator LBH" (in en). Biochemical and Biophysical Research Communications 391 (1): 1104–1109. doi:10.1016/j.bbrc.2009.12.032. ISSN 0006-291X. PMID 20005203. 
  6. ↑ Camacho-Zarco, Aldo R.; Schnapka, Vincent; Guseva, Serafima; Abyzov, Anton; Adamski, Wiktor; Milles, Sigrid; Jensen, Malene Ringkjøbing; Zidek, Lukas et al. (2022-04-21). "NMR Provides Unique Insight into the Functional Dynamics and Interactions of Intrinsically Disordered Proteins". Chemical Reviews 122 (10): 9331–9356. doi:10.1021/acs.chemrev.1c01023. ISSN 1520-6890. PMID 35446534. 
  7. ↑ Rao, Tata Purushothama; Kühl, Michael (2010-06-25). "An updated overview on Wnt signaling pathways: a prelude for more". Circulation Research 106 (12): 1798–1806. doi:10.1161/CIRCRESAHA.110.219840. ISSN 1524-4571. PMID 20576942. 
  8. ↑ Francke, Uta (1976-11-01). "The 2p Partial Trisomy Syndrome: Duplication of Region 2p23 → 2pter in Two Members of a t(2;7) Translocation Kindred" (in en). American Journal of Diseases of Children 130 (11): 1244–1249. doi:10.1001/archpedi.1976.02120120078014. ISSN 0002-922X. PMID 984008. http://archpedi.jamanetwork.com/article.aspx?doi=10.1001/archpedi.1976.02120120078014. 
  9. ↑ Briegel, Karoline J.; Baldwin, H. Scott; Epstein, Jonathan A.; Joyner, Alexandra L. (2005-07-15). "Congenital heart disease reminiscent of partial trisomy 2p syndrome in mice transgenic for the transcription factor Lbh" (in en). Development 132 (14): 3305–3316. doi:10.1242/dev.01887. ISSN 1477-9129. PMID 15958514. https://journals.biologists.com/dev/article/132/14/3305/18524/Congenital-heart-disease-reminiscent-of-partial. 
  10. ↑ Ashad-Bishop, Kilan; Garikapati, Koteswararao; Lindley, Linsey E.; Jorda, Merce; Briegel, Karoline J. (January 2019). "Loss of Limb-Bud-and-Heart (LBH) attenuates mammary hyperplasia and tumor development in MMTV-Wnt1 transgenic mice" (in en). Biochemical and Biophysical Research Communications 508 (2): 536–542. doi:10.1016/j.bbrc.2018.11.155. PMID 30509497. 

Further reading




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