» Articles » PMID: 20463047

Parallel Retention of Pdx2 Genes in Cartilaginous Fish and Coelacanths

Overview
Journal Mol Biol Evol
Specialty Biology
Date 2010 May 14
PMID 20463047
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

The Pdx1 or Ipf1 gene encodes an important homeodomain-containing protein with key roles in pancreas development and function. Mutations in human PDX1 are implicated in developmental defects and disease of the pancreas. Extensive research, including genome sequencing, has indicated that Pdx1 is the only member of its gene family in mammals, birds, amphibians, and ray-finned fish, and with the exception of teleost fish, this gene forms part of the ParaHox gene cluster along with Gsx1 and Cdx2. The ParaHox cluster, however, is a remnant of a 4-fold genome duplication; the three other ParaHox paralogues lack a Pdx-like gene in all vertebrate genomes examined to date. We have used bacterial artificial chromosome cloning and synteny analysis to show that the ancestor of living jawed vertebrates in fact had more ParaHox genes, including two Pdx genes (Pdx1 and Pdx2). Surprisingly, the two Pdx genes have been retained in parallel in two quite distantly related lineages, the cartilaginous fish (sharks, skates, and chimeras) and the Indonesian coelacanth, Latimeria menadoensis. The Pdx2 gene has been lost independently in ray-finned fish and in tetrapods.

Citing Articles

Revealing the biological features of the axolotl pancreas as a new research model.

Ma H, Peng G, Hu Y, Lu B, Zheng Y, Wu Y Front Cell Dev Biol. 2025; 13:1531903.

PMID: 39958891 PMC: 11825805. DOI: 10.3389/fcell.2025.1531903.


Evidence from oyster suggests an ancient role for Pdx in regulating insulin gene expression in animals.

Xu F, Marletaz F, Gavriouchkina D, Liu X, Sauka-Spengler T, Zhang G Nat Commun. 2021; 12(1):3117.

PMID: 34035261 PMC: 8149454. DOI: 10.1038/s41467-021-23216-7.


Lampreys, the jawless vertebrates, contain only two ParaHox gene clusters.

Zhang H, Ravi V, Tay B, Tohari S, Pillai N, Prasad A Proc Natl Acad Sci U S A. 2017; 114(34):9146-9151.

PMID: 28784804 PMC: 5576799. DOI: 10.1073/pnas.1704457114.


The small non-coding RNA processing machinery of two living fossil species, lungfish and coelacanth, gives new insights into the evolution of the Argonaute protein family.

Biscotti M, Canapa A, Forkoni M, Gerdol M, Pallavicini A, Schartl M Genome Biol Evol. 2017; 9(3):438-453.

PMID: 28206606 PMC: 5381642. DOI: 10.1093/gbe/evx017.


The spotted gar genome illuminates vertebrate evolution and facilitates human-teleost comparisons.

Braasch I, Gehrke A, Smith J, Kawasaki K, Manousaki T, Pasquier J Nat Genet. 2016; 48(4):427-37.

PMID: 26950095 PMC: 4817229. DOI: 10.1038/ng.3526.


References
1.
Cockburn B, Bermano G, Boodram L, Teelucksingh S, Tsuchiya T, Mahabir D . Insulin promoter factor-1 mutations and diabetes in Trinidad: identification of a novel diabetes-associated mutation (E224K) in an Indo-Trinidadian family. J Clin Endocrinol Metab. 2004; 89(2):971-8. DOI: 10.1210/jc.2003-031282. View

2.
Lynch M, Force A . The probability of duplicate gene preservation by subfunctionalization. Genetics. 2000; 154(1):459-73. PMC: 1460895. DOI: 10.1093/genetics/154.1.459. View

3.
Illes J, Winterbottom E, Isaacs H . Cloning and expression analysis of the anterior parahox genes, Gsh1 and Gsh2 from Xenopus tropicalis. Dev Dyn. 2008; 238(1):194-203. DOI: 10.1002/dvdy.21816. View

4.
Ohlsson H, Karlsson K, Edlund T . IPF1, a homeodomain-containing transactivator of the insulin gene. EMBO J. 1993; 12(11):4251-9. PMC: 413720. DOI: 10.1002/j.1460-2075.1993.tb06109.x. View

5.
Jonsson J, Carlsson L, Edlund T, Edlund H . Insulin-promoter-factor 1 is required for pancreas development in mice. Nature. 1994; 371(6498):606-9. DOI: 10.1038/371606a0. View