Literature DB >> 9524228

Analysis of the murine Hoxa-9 cDNA: an alternatively spliced transcript encodes a truncated protein lacking the homeodomain.

S Fujimoto1, K Araki, O Chisaka, M Araki, K Takagi, K Yamamura.   

Abstract

Hoxa-9 is one of the homeo box (Hox) genes exhibiting similarity to the Drosophila Abdominal B gene. So far, only partial nucleotide sequences have been reported for mouse Hoxa-9 cDNA (Rubin et al., (1987) Mol. Cell. Biol. 7, 3836-3841). Here, we have determined the nucleotide sequence of the 5'-region of mouse Hoxa-9 cDNA and its genomic structure. Mouse Hoxa-9 cDNA contains a complete ORF encoding a protein of 271aa exhibiting 96.7% identity to its human counterpart. Interestingly, an alternatively spliced transcript (Hoxa-9T) was identified by RT-PCR. Sequence analysis revealed that 173bp within the Hoxa-9 ORF was missing from the Hoxa-9T cDNA. This additional splicing would potentially result in a frameshift, leading to the production of a truncated protein lacking the homeobox. Northern blot analysis revealed that the probe containing the homeodomain hybridized to two major transcripts (2.5 and 1.9kb) in the trunk region of 12.5 dpc embryos, and adult kidney and large intestine. On the other hand, the probe containing the additional intron detected only 2.5kb transcript in the same tissues, indicating that 1.9kb transcript corresponds to Hoxa-9T mRNA. We have also determined the transcriptional start site of Hoxa-9T.

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Year:  1998        PMID: 9524228     DOI: 10.1016/s0378-1119(98)00014-6

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  14 in total

1.  Conservation of the TGFbeta/Labial homeobox signaling loop in endoderm-derived cells between Drosophila and mammals.

Authors:  Gwen A Lomberk; Issei Imoto; Brian Gebelein; Raul Urrutia; Tiffany A Cook
Journal:  Pancreatology       Date:  2010-03-26       Impact factor: 3.996

Review 2.  Transcriptional complexity of the HOXA9 locus.

Authors:  Relja Popovic; Frank Erfurth; Nancy Zeleznik-Le
Journal:  Blood Cells Mol Dis       Date:  2007-10-03       Impact factor: 3.039

3.  Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families.

Authors:  F Goodman; M L Giovannucci-Uzielli; C Hall; W Reardon; R Winter; P Scambler
Journal:  Am J Hum Genet       Date:  1998-10       Impact factor: 11.025

4.  MLL associates specifically with a subset of transcriptionally active target genes.

Authors:  Thomas A Milne; Yali Dou; Mary Ellen Martin; Hugh W Brock; Robert G Roeder; Jay L Hess
Journal:  Proc Natl Acad Sci U S A       Date:  2005-09-30       Impact factor: 11.205

5.  Two isoforms of HOXA9 function differently but work synergistically in human MLL-rearranged leukemia.

Authors:  Miao He; Ping Chen; Stephen Arnovitz; Yuanyuan Li; Hao Huang; Mary Beth Neilly; Minjie Wei; Janet D Rowley; Jianjun Chen; Zejuan Li
Journal:  Blood Cells Mol Dis       Date:  2012-05-25       Impact factor: 3.039

6.  Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.

Authors:  M Alders; A Ryan; M Hodges; J Bliek; A P Feinberg; O Privitera; A Westerveld; P F Little; M Mannens
Journal:  Am J Hum Genet       Date:  2000-04-10       Impact factor: 11.025

7.  MicroRNA-126 regulates HOXA9 by binding to the homeobox.

Authors:  Wei-Fang Shen; Yu-Long Hu; Lalita Uttarwar; Emmanuelle Passegue; Corey Largman
Journal:  Mol Cell Biol       Date:  2008-05-12       Impact factor: 4.272

8.  The truncated Hoxa1 protein interacts with Hoxa1 and Pbx1 in stem cells.

Authors:  Cristina C Fernandez; Lorraine J Gudas
Journal:  J Cell Biochem       Date:  2009-02-15       Impact factor: 4.429

9.  The leukemogenicity of Hoxa9 depends on alternative splicing.

Authors:  C R Stadler; N Vegi; M A Mulaw; K E Edmaier; V P S Rawat; A Dolnik; L Bullinger; B Heilmeier; L Quintanilla-Fend; K Spiekermann; W Hiddemann; K Döhner; H Döhner; M Feuring-Buske; C Buske
Journal:  Leukemia       Date:  2014-02-18       Impact factor: 11.528

10.  Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina).

Authors:  Agnès Burel; Thomas Mouchel; Sylvie Odent; Filiz Tiker; Bertrand Knebelmann; Isabelle Pellerin; Daniel Guerrier
Journal:  J Negat Results Biomed       Date:  2006-03-23
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