Literature DB >> 1360670

Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4.

H S Stadler1, B J Padanilam, K Buetow, J C Murray, M Solursh.   

Abstract

A human craniofacial cDNA library was screened with a degenerate oligonucleotide probe based on the conserved third helix of homeobox genes. From this screening, we identified a homeobox gene, H6, which shared only 57-65% amino acid identity to previously reported homeodomains. H6 was physically mapped to the 4p16.1 region by using somatic cell hybrids containing specific deletions of human chromosome 4. Linkage data from a single-stranded conformational polymorphism derived from the 3' untranslated region of the H6 cDNA placed this homeobox gene more than 20 centimorgans proximal of the previously mapped HOX7 gene on chromosome 4. Identity comparisons of the H6 homeodomain with previously reported homeodomains reveal the highest identities to be with the Nk class of homeobox genes in Drosophila melanogaster.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1360670      PMCID: PMC50596          DOI: 10.1073/pnas.89.23.11579

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  50 in total

1.  Genetic and physical maps of human chromosome 4 based on dinucleotide repeats.

Authors:  K A Mills; K H Buetow; Y Xu; J L Weber; M R Altherr; J J Wasmuth; J C Murray
Journal:  Genomics       Date:  1992-10       Impact factor: 5.736

2.  Molecular Genetics of the Bithorax Complex in Drosophila melanogaster.

Authors:  W Bender; M Akam; F Karch; P A Beachy; M Peifer; P Spierer; E B Lewis; D S Hogness
Journal:  Science       Date:  1983-07-01       Impact factor: 47.728

3.  Screening lambdagt recombinant clones by hybridization to single plaques in situ.

Authors:  W D Benton; R W Davis
Journal:  Science       Date:  1977-04-08       Impact factor: 47.728

4.  Base composition-independent hybridization in tetramethylammonium chloride: a method for oligonucleotide screening of highly complex gene libraries.

Authors:  W I Wood; J Gitschier; L A Lasky; R M Lawn
Journal:  Proc Natl Acad Sci U S A       Date:  1985-03       Impact factor: 11.205

5.  A mouse gene homologous to the Drosophila gene caudal is expressed in epithelial cells from the embryonic intestine.

Authors:  P Duprey; K Chowdhury; G R Dressler; R Balling; D Simon; J L Guenet; P Gruss
Journal:  Genes Dev       Date:  1988-12       Impact factor: 11.361

6.  Organization of human homeobox genes.

Authors:  E Boncinelli; R Somma; D Acampora; M Pannese; M D'Esposito; A Faiella; A Simeone
Journal:  Hum Reprod       Date:  1988-10       Impact factor: 6.918

7.  Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene hox-1.5.

Authors:  O Chisaka; M R Capecchi
Journal:  Nature       Date:  1991-04-11       Impact factor: 49.962

8.  A conserved DNA sequence in homoeotic genes of the Drosophila Antennapedia and bithorax complexes.

Authors:  W McGinnis; M S Levine; E Hafen; A Kuroiwa; W J Gehring
Journal:  Nature       Date:  1984 Mar 29-Apr 4       Impact factor: 49.962

9.  Developmental defects of the ear, cranial nerves and hindbrain resulting from targeted disruption of the mouse homeobox gene Hox-1.6.

Authors:  O Chisaka; T S Musci; M R Capecchi
Journal:  Nature       Date:  1992-02-06       Impact factor: 49.962

10.  Developmental and molecular analysis of Deformed; a homeotic gene controlling Drosophila head development.

Authors:  M Regulski; N McGinnis; R Chadwick; W McGinnis
Journal:  EMBO J       Date:  1987-03       Impact factor: 11.598

View more
  6 in total

1.  The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.

Authors:  S T Winokur; U Bengtsson; J Feddersen; K D Mathews; B Weiffenbach; H Bailey; R P Markovich; J C Murray; J J Wasmuth; M R Altherr
Journal:  Chromosome Res       Date:  1994-05       Impact factor: 5.239

2.  Assignment of the murine Hmx1 homeobox gene to the proximal region of mouse chromosome 5.

Authors:  W Wang; K Yoshiura; J Murray; T Lufkin
Journal:  Mamm Genome       Date:  1997       Impact factor: 2.957

3.  Phylogenetic conservation and physical mapping of members of the H6 homeobox gene family.

Authors:  H S Stadler; J C Murray; N J Leysens; P J Goodfellow; M Solursh
Journal:  Mamm Genome       Date:  1995-06       Impact factor: 2.957

4.  Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome.

Authors:  Daniel F Schorderet; Olivia Nichini; Gaëlle Boisset; Bozena Polok; Leila Tiab; Hélène Mayeur; Bahija Raji; Gauillaume de la Houssaye; Marc M Abitbol; Francis L Munier
Journal:  Am J Hum Genet       Date:  2008-05       Impact factor: 11.025

5.  MSX1 polymorphism associated with risk of oral cleft in Korea: evidence from case-parent trio and case-control studies.

Authors:  Jungyong Park; Beyoung Yun Park; Hyon-Suk Kim; Jong Eun Lee; Il Suh; Chung Mo Nam; Dae Ryong Kang; Suk Kim; Ji Eun Yun; Eun Na Go; Sun Ha Jee; Terri H Beaty
Journal:  Yonsei Med J       Date:  2007-02-28       Impact factor: 2.759

6.  A dimerized HMX1 inhibits EPHA6/epha4b in mouse and zebrafish retinas.

Authors:  Fabienne Marcelli; Gaëlle Boisset; Daniel F Schorderet
Journal:  PLoS One       Date:  2014-06-19       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.