Literature DB >> 1685479

Structure and sequence of the human homeobox gene HOX7.

J E Hewitt1, L N Clark, A Ivens, R Williamson.   

Abstract

A cosmid containing the human sequence HOX7, homologous to the murine Hox-7 gene, was isolated from a genomic library, and the positions of the coding sequences were determined by hybridization. DNA sequence analysis demonstrated two exons that code for a homeodomain-containing protein of 297 amino acids. The open reading frame is interrupted by a single intron of approximately 1.6 kb, the splice donor and acceptor sites of which conform to known consensus sequences. The human HOX7 coding sequence has a very high degree of identity with the murine Hox-7 cDNA. Within the homeobox, the two sequences share 94% identity at the DNA level, all substitutions being silent. This high level of sequence similarity is not confined to the homeodomain; overall the human and murine HOX7 gene products show 80% identity at the amino acid level. Both the 5' and 3' untranslated regions also show significant similarity to the murine gene, with 79 and 70% sequence identity, respectively. The sequence upstream of the coding sequence of exon 1 contains a GC-rich putative promoter region. There is no TATA box, but a CCAAT and numerous GC boxes are present. The region encompassing the promoter region, exon 1, and the 5' region of exon 2 have a higher than expected frequency of CpG dinucleotides; numerous sites for rare-cutter restriction enzymes are present, a characteristic of HTF islands.

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Year:  1991        PMID: 1685479     DOI: 10.1016/0888-7543(91)90074-o

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


  21 in total

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

Authors:  H S Stadler; B J Padanilam; K Buetow; J C Murray; M Solursh
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-01       Impact factor: 11.205

2.  Gestational exposure to ethanol suppresses msx2 expression in developing mouse embryos.

Authors:  L Rifas; D A Towler; L V Avioli
Journal:  Proc Natl Acad Sci U S A       Date:  1997-07-08       Impact factor: 11.205

3.  A novel homeobox gene mediates the Dpp signal to establish functional specificity within target cells.

Authors:  H Nakagoshi; M Hoshi; Y Nabeshima; F Matsuzaki
Journal:  Genes Dev       Date:  1998-09-01       Impact factor: 11.361

4.  Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia.

Authors:  Munefumi Kamamoto; Junichiro Machida; Seishi Yamaguchi; Masashi Kimura; Takao Ono; Peter A Jezewski; Yujiro Higashi; Atsuo Nakayama; Kazuo Shimozato; Yoshihito Tokita
Journal:  Eur J Hum Genet       Date:  2011-03-30       Impact factor: 4.246

5.  Sensitivity of HincII to CpG methylation.

Authors:  L N Bull; J E Hewitt; D R Cox; R M Myers
Journal:  Nucleic Acids Res       Date:  1993-04-25       Impact factor: 16.971

6.  A nonsense mutation in MSX1 causes Witkop syndrome.

Authors:  D Jumlongras; M Bei; J M Stimson; W F Wang; S R DePalma; C E Seidman; U Felbor; R Maas; J G Seidman; B R Olsen
Journal:  Am J Hum Genet       Date:  2001-05-16       Impact factor: 11.025

7.  Structure of the gene encoding hepatocyte nuclear factor 1 (HNF1).

Authors:  I Bach; M Pontoglio; M Yaniv
Journal:  Nucleic Acids Res       Date:  1992-08-25       Impact factor: 16.971

8.  Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

Authors:  A C Lidral; P A Romitti; A M Basart; T Doetschman; N J Leysens; S Daack-Hirsch; E V Semina; L R Johnson; J Machida; A Burds; T J Parnell; J L Rubenstein; J C Murray
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

9.  The role of MSX1 in human tooth agenesis.

Authors:  A C Lidral; B C Reising
Journal:  J Dent Res       Date:  2002-04       Impact factor: 6.116

10.  Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16.

Authors:  Luc Djoussé; Beth Knowlton; Michael R Hayden; Elisabeth W Almqvist; Ryan R Brinkman; Christopher A Ross; Russel L Margolis; Adam Rosenblatt; Alexandra Durr; Catherine Dode; Patrick J Morrison; Andrea Novelletto; Marina Frontali; Ronald J A Trent; Elizabeth McCusker; Estrella Gómez-Tortosa; David Mayo Cabrero; Randi Jones; Andrea Zanko; Martha Nance; Ruth K Abramson; Oksana Suchowersky; Jane S Paulsen; Madaline B Harrison; Qiong Yang; L Adrienne Cupples; Jayalakshmi Mysore; James F Gusella; Marcy E MacDonald; Richard H Myers
Journal:  Neurogenetics       Date:  2004-03-17       Impact factor: 2.660

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