Literature DB >> 7910581

Genomic organization and chromosome localization of the murine homeobox gene Pmx.

M J Kern1, E A Argao, E H Birkenmeier, L B Rowe, S S Potter.   

Abstract

Homeobox genes are expressed in very specific temporal and spatial patterns and function as transcriptional regulators of developmental processes. The murine homeobox gene, Pmx (paired mesoderm homeobox), is expressed in a mesodermally restricted pattern in embryos and most abundantly in cardiac, skeletal, and smooth muscle tissues in adults. Previously, this murine gene was named K-2 and mHox, while the human homolog was named Phox1. In this report, the localization of Pmx has been determined by interspecific backcross analysis. The Pmx gene is located on Chromosome 1, approximately 3.3 cM distal to the Gsh-4 homeobox locus. The sequence of the Pmx transcript has been extended toward the 5' end and corresponds in size to one of the transcripts previously detected by Northern blot analysis. Sequence analysis indicates that Pmx is the first characterized mammalian gene to encode a paired type homeodomain, but not a paired domain. The Pmx gene includes at least five exons spanning a minimum of 60 kb of genomic DNA, making this the largest known murine homeobox gene.

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Year:  1994        PMID: 7910581     DOI: 10.1006/geno.1994.1066

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  9 in total

1.  Maps from two interspecific backcross DNA panels available as a community genetic mapping resource.

Authors:  L B Rowe; J H Nadeau; R Turner; W N Frankel; V A Letts; J T Eppig; M S Ko; S J Thurston; E H Birkenmeier
Journal:  Mamm Genome       Date:  1994-05       Impact factor: 2.957

2.  Notochordal and foregut abnormalities correlate with elevated neural crest apoptosis in Patch embryos.

Authors:  Paige Snider; Olga Simmons; Rhonda Rogers; Rachel Young; Mica Gosnell; Simon J Conway
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2011-05-06

3.  PRRX-NCOA1/2 rearrangement characterizes a distinctive fibroblastic neoplasm.

Authors:  Maribel D Lacambra; Ilan Weinreb; Elizabeth G Demicco; Chit Chow; Yun-Shao Sung; David Swanson; Ka-Fai To; Kwok-Chuen Wong; Cristina R Antonescu; Brendan C Dickson
Journal:  Genes Chromosomes Cancer       Date:  2019-04-30       Impact factor: 5.006

4.  PRRX1 isoform PRRX1A regulates the stemness phenotype and epithelial-mesenchymal transition (EMT) of cancer stem-like cells (CSCs) derived from non-small cell lung cancer (NSCLC).

Authors:  Lei Sun; Tao Han; Xinyu Zhang; Xiangli Liu; Peiwen Li; Mingrui Shao; Siyuan Dong; Wenya Li
Journal:  Transl Lung Cancer Res       Date:  2020-06

5.  Gsh-1, an orphan Hox gene, is required for normal pituitary development.

Authors:  H Li; P S Zeitler; M T Valerius; K Small; S S Potter
Journal:  EMBO J       Date:  1996-02-15       Impact factor: 11.598

6.  Modifiers of hearing impairment in humans and mice.

Authors:  Denise Yan; Xue-Zhong Liu
Journal:  Curr Genomics       Date:  2010-06       Impact factor: 2.236

7.  Expanding the spectrum of SMAD3-related phenotypes to agnathia-otocephaly.

Authors:  Nicole Meier; Elisabeth Bruder; Peter Miny; Sevgi Tercanli; Isabel Filges
Journal:  Mol Genet Genomic Med       Date:  2020-02-26       Impact factor: 2.183

8.  Stable transmission of complex chromosomal rearrangements involving chromosome 1q derived from constitutional chromoanagenesis.

Authors:  Mary A Gudipati; Elizabeth Waters; Carol Greene; Nidhi Goel; Nicole L Hoppman; Beth A Pitel; Matthew R Webley; Ying Zou
Journal:  Mol Cytogenet       Date:  2019-10-31       Impact factor: 2.009

9.  Transcription factor paired related homeobox 1 (PRRX1) activates matrix metalloproteinases (MMP)13, which promotes the dextran sulfate sodium-induced inflammation and barrier dysfunction of NCM460 cells.

Authors:  Xiujing Zhang; Lizhuan Ma; Ying Shen; Chao Zhang; Bingxu Hou; Yanli Zhou
Journal:  Bioengineered       Date:  2022-01       Impact factor: 3.269

  9 in total

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