PDX1

{{Short description|A protein involved in the pancreas and duodenum differentiation}}

PDX1 (pancreatic and duodenal homeobox 1), also known as insulin promoter factor 1, is a transcription factor in the ParaHox gene cluster.Brooke, N. M., Garcia-Fernàndez, J., & Holland, P. W. (1998). The ParaHox gene cluster is an evolutionary sister of the Hox gene cluster. Nature, 392(6679), 920. In vertebrates, Pdx1 is necessary for pancreatic development, including β-cell maturation, and duodenal differentiation. In humans this protein is encoded by the PDX1 gene, which was formerly known as IPF1.{{cite web|title=PDX1|url=https://www.genenames.org/cgi-bin/gene_symbol_report?hgnc_id=6107|website=HGNC|access-date=22 April 2016|archive-date=3 March 2016|archive-url=https://web.archive.org/web/20160303225837/http://www.genenames.org/cgi-bin/gene_symbol_report?hgnc_id=6107|url-status=dead}}{{cite journal | vauthors = Stoffel M, Stein R, Wright CV, Espinosa R, Le Beau MM, Bell GI | title = Localization of human homeodomain transcription factor insulin promoter factor 1 (IPF1) to chromosome band 13q12.1 | journal = Genomics | volume = 28 | issue = 1 | pages = 125–6 |date=July 1995 | pmid = 7590740 | doi = 10.1006/geno.1995.1120 }} The gene was originally identified in the clawed frog Xenopus laevis Wright, C. V., Schnegelsberg, P., & De Robertis, E. M. (1989). XlHbox 8: a novel Xenopus homeo protein restricted to a narrow band of endoderm. Development, 105(4), 787-794. and is present widely across the evolutionary diversity of bilaterian animals, although it has been lost in evolution in arthropods and nematodes. Despite the gene name being Pdx1, there is no Pdx2 gene in most animals; single-copy Pdx1 orthologs have been identified in all mammals.{{cite web | title = OrthoMaM phylogenetic marker: PDX1 coding sequence | url = http://www.orthomam.univ-montp2.fr/orthomam_v10b/cds/GenerateDetailMarkers/ENSG00000139515_PDX1.html | date = 2019 | website = OrthoMam v10 | access-date = 24 February 2019 }} Coelacanth and cartilaginous fish are, so far, the only vertebrates shown to have two Pdx genes, Pdx1 and Pdx2.{{cite journal | vauthors = Mulley JF, Holland PW | title = Parallel retention of Pdx2 genes in cartilaginous fish and coelacanths | journal = Molecular Biology and Evolution | volume = 27 | issue = 10 | pages = 2386–91 | date = October 2010 | pmid = 20463047 | doi = 10.1093/molbev/msq121 | pmc = 2944030 | doi-access = free }}

Function

= Pancreatic development =

In pancreatic development, Pdx1 is expressed by a population of cells in the posterior foregut region of the definitive endoderm, and Pdx1⁺ epithelial cells give rise to the developing pancreatic buds, and eventually, the whole of the pancreas—its exocrine, endocrine, and ductal cell populations.{{cite journal | vauthors = D'Amour KA, Bang AG, Eliazer S, Kelly OG, Agulnick AD, Smart NG, Moorman MA, Kroon E, Carpenter MK, Baetge EE | title = Production of pancreatic hormone-expressing endocrine cells from human embryonic stem cells | journal = Nat. Biotechnol. | volume = 24 | issue = 11 | pages = 1392–401 |date=November 2006 | pmid = 17053790 | doi = 10.1038/nbt1259 | s2cid = 11040949 }} Pancreatic Pdx1⁺ cells first arise at mouse embryonic day 8.5-9.0 (E8.5-9.0), and Pdx1 expression continues until E12.0-E12.5.{{cite journal | vauthors = Stanger BZ, Tanaka AJ, Melton DA | title = Organ size is limited by the number of embryonic progenitor cells in the pancreas but not the liver | journal = Nature | volume = 445 | issue = 7130 | pages = 886–91 |date=February 2007 | pmid = 17259975 | doi = 10.1038/nature05537 | bibcode = 2007Natur.445..886S | s2cid = 4379651 }} Homozygous Pdx1 knockout mice form pancreatic buds but fail to develop a pancreas, and transgenic mice in which tetracycline application results in death of Pdx1⁺ cells are almost completely apancreatic if doxycycline (tetracycline derivative) is administered throughout the pregnancy of these transgenic mice, illustrating the necessity of Pdx1⁺ cells in pancreatic development.

Pdx1 is accepted as the earliest marker for pancreatic differentiation, with the fates of pancreatic cells controlled by downstream transcription factors.{{cite journal | vauthors = Liew CG, Shah NN, Briston SJ, Shepherd RM, Khoo CP, Dunne MJ, Moore HD, Cosgrove KE, Andrews PW | title = PAX4 enhances beta-cell differentiation of human embryonic stem cells | journal = PLOS ONE | volume = 3 | issue = 3 | pages = e1783 | year = 2008 | pmid = 18335054 | pmc = 2262135 | doi = 10.1371/journal.pone.0001783 | bibcode = 2008PLoSO...3.1783L | doi-access = free }} {{open access}} The initial pancreatic bud is composed of Pdx1⁺ pancreatic progenitor cells that co-express Hlxb9, Hnf6, Ptf1a and NKX6-1. These cells further proliferate and branch in response to FGF-10 signaling. Afterwards, differentiation of the pancreatic cells begins; a population of cells has Notch signaling inhibited, and subsequently, expresses Ngn3. This Ngn3⁺ population is a transient population of pancreatic endocrine progenitors that gives rise to the α, β, Δ, PP, and ε cells of the islets of Langerhans. Other cells will give rise to the exocrine and ductal pancreatic cell populations.

= β-cell maturation and survival =

The final stages of pancreas development involves the production of different endocrine cells, including insulin-producing β-cells and glucagon-producing α-cells. Pdx1 is necessary for β-cell maturation: developing β-cells co-express Pdx1, NKX6-1, and insulin, a process that results in the silencing of MafB and the expression of MafA, a necessary switch in maturation of β-cells. At this stage of pancreas development, the experimental decrease in the expression of Pdx1 results in a production of a smaller number of β-cells and an associated increase in the number of α-cells. Gannon M, Ables ET, Crawford L, et al. pdx-1 function is specifically required in embryonic beta cells to generate appropriate numbers of endocrine cell types and maintain glucose homeostasis. Dev Biol. 2007;314(2):406-17. doi:10.1016/j.ydbio.2007.10.038

In the mature pancreas, Pdx1 expression seems to be required for the maintenance and survival of β-cells. For instance, experimentally reducing the level of Pdx1 expression at this stage makes β-cells produce higher amounts of glucagon,Ahlgren U, Jonsson J, Jonsson L, Simu K, Edlund H. beta-cell-specific inactivation of the mouse Ipf1/Pdx1 gene results in loss of the beta-cell phenotype and maturity onset diabetes. Genes Dev. 1998;12(12):1763-8. suggesting that Pdx1 inhibits the conversion of β-cells into α-cells. Furthermore, Pdx1 appears to be important in mediating the effect of insulin on the apoptotic programmed cell death of β-cells: a small concentration of insulin protects β-cells from apoptosis, but not in cells where Pdx1 expression has been inhibited.{{cite journal | vauthors = Johnson JD, Ahmed NT, Luciani DS, Han Z, Tran H, Fujita J, Misler S, Edlund H, Polonsky KS | title = Increased islet apoptosis in Pdx1+/- mice | journal = J. Clin. Invest. | volume = 111 | issue = 8 | pages = 1147–60 |date=April 2003 | pmid = 12697734 | pmc = 152933 | doi = 10.1172/JCI16537 }}{{cite journal | vauthors = Johnson JD, Bernal-Mizrachi E, Alejandro EU, Han Z, Kalynyak TB, Li H, Beith JL, Gross J, Warnock GL, Townsend RR, Permutt MA, Polonsky KS | title = Insulin protects islets from apoptosis via Pdx1 and specific changes in the human islet proteome | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 103 | issue = 51 | pages = 19575–80 |date=December 2006 | pmid = 17158802 | pmc = 1748267 | doi = 10.1073/pnas.0604208103 | bibcode = 2006PNAS..10319575J | doi-access = free }}

= Duodenum =

Pdx1 is necessary for the development of the proximal duodenum and maintenance of the gastro-duodenal junction.{{cite journal |vauthors=Holland AM, Garcia S, Naselli G, Macdonald RJ, Harrison LC |title=The Parahox gene Pdx1 is required to maintain positional identity in the adult foregut |journal=Int. J. Dev. Biol. |volume=57 |issue=5 |pages=391–8 |year=2013 |pmid=23873371 |doi=10.1387/ijdb.120048ah |url=http://www.ijdb.ehu.es/web/descarga/paper/120048ah|doi-access=free }} Duodenal enterocytes, Brunner's glands and entero-endocrine cells (including those in the gastric antrum) are dependent on Pdx1 expression. It is a ParaHox gene, which together with Sox2 and Cdx2, determines the correct cellular differentiation in the proximal gut. In mature mice duodenum, several genes have been identified which are dependent on Pdx1 expression and include some affecting lipid and iron absorption.{{cite journal |vauthors=Chen C, Sibley E |title=Expression profiling identifies novel gene targets and functions for Pdx1 in the duodenum of mature mice |journal=Am. J. Physiol. Gastrointest. Liver Physiol. |volume=302 |issue=4 |pages=G407–19 |year=2012 |pmid=22135308 |pmc=3287393 |doi=10.1152/ajpgi.00314.2011 }}

Pathology

Experiments in animal models have shown that a reduction in Pdx1 expression can cause symptoms that are characteristic of Diabetes mellitus type 1 and Diabetes mellitus type 2.Fujimoto, Kei, and Kenneth S. Polonsky. "Pdx1 and other factors that regulate pancreatic β‐cell survival." Diabetes, Obesity and Metabolism 11 (2009): 30-37. Furthermore, expression of Pdx1 is lost in gastric cancers, suggesting a role for the gene as a tumor suppressor.{{cite journal |vauthors=Ma J, Chen M, Wang J, Xia HH, Zhu S, Liang Y, Gu Q, Qiao L, Dai Y, Zou B, Li Z, Zhang Y, Lan H, Wong BC |title=Pancreatic duodenal homeobox-1 (PDX1) functions as a tumor suppressor in gastric cancer |journal=Carcinogenesis |volume=29 |issue=7 |pages=1327–33 |year=2008 |pmid=18477649 |doi=10.1093/carcin/bgn112 |doi-access=free }} Maturity onset diabetes of the young (Type 4) can be caused by heterozygous mutations in Pdx1.{{cite web | title = Entrez Gene: PDX1 pancreatic and duodenal homeobox 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3651}}{{cite journal | vauthors = Fajans SS, Bell GI, Polonsky KS | title = Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young | journal = N. Engl. J. Med. | volume = 345 | issue = 13 | pages = 971–80 |date=September 2001 | pmid = 11575290 | doi = 10.1056/NEJMra002168 }} The fat sand rat Psammomys obesus, a species with susceptibility to Diabetes mellitus type 2 symptoms, has a highly divergent Pdx1 gene sequence compared with other mammals.{{cite journal | vauthors = Hargreaves AD, Zhou L, Christensen J, Marlétaz F, Liu S, Li F, Jansen PG, Spiga E, Hansen MT, Pedersen SV, Biswas S, Serikawa K, Fox BA, Taylor WR, Mulley JF, Zhang G, Heller RS, Holland PW | display-authors = 6 | title = Genome sequence of a diabetes-prone rodent reveals a mutation hotspot around the ParaHox gene cluster | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 114 | issue = 29 | pages = 7677–7682 | date = July 2017 | pmid = 28674003 | pmc = 5530673 | doi = 10.1073/pnas.1702930114 | bibcode = 2017PNAS..114.7677H | doi-access = free }}

Interactions

Pdx1 has been shown to interact with MAFA.{{cite journal | vauthors = Zhao L, Guo M, Matsuoka TA, Hagman DK, Parazzoli SD, Poitout V, Stein R | title = The islet beta cell-enriched MafA activator is a key regulator of insulin gene transcription | journal = J. Biol. Chem. | volume = 280 | issue = 12 | pages = 11887–94 |date=March 2005 | pmid = 15665000 | doi = 10.1074/jbc.M409475200 | doi-access = free }}

References

External links

[https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=dmn GeneReviews/NCBI/NIH/UW entry on Permanent Neonatal Diabetes Mellitus]
{{MeshName|PDX1+protein,+human}}

Category:Transcription factors