Katoh Masuko, Katoh Masaru
M&M Medical BioInformatics, Narashino 275-0022, Japan.
Int J Oncol. 2004 May;24(5):1339-44.
Forkhead-box (FOX) genes are implicated in embryogenesis through transcriptional regulation depending on SHH-GLI pathway, TGF-beta pathway etc., and also in carcinogenesis through gene amplification, retroviral integration and chromosomal translocation. FOXN1, FOXN2 (HTLF), FOXN3 (CHES1) and FOXN4 constitute the FOXN family. Here, we identified and characterized the FOXN5 gene, a novel member of FOXN gene family, by using bioinformatics. IMAGE5167039 (BC028191.1) was the representative cDNA derived from human FOXN5 gene. Rat Foxn5 gene, consisting of six exons, was identified within rat genome sequence CH230-26K11 (AC107575.5). Complete coding sequence of rat Foxn5 cDNA was determined by assembling nucleotide sequences of rat Foxn5 exons. Human FOXN5 (292 aa) and rat Foxn5 (296 aa) showed 77.4% total-amino-acid identity. Codon 173-254 of FOXN5 was the Forkhead domain. FOXN5 gene, consisting of six exons, was linked to BCL9L gene at human chromosome 11q23.3. FOXN5 is a candidate tumor suppressor gene (TSG), just like ARHGAP20 (KIAA1391), BTG4, SNF1LK2 (SIK2), DIXDC1 (KIAA1735) genes at 11q23.1, TTC12 (TPARM) gene at 11q23.2, IGSF4, DSCAML1, LL5A (PHLDB1), BCL9L, RNF26, and MFRP genes at 11q23.3. This is the first report on the human FOXN5 and rat Foxn5 genes.
叉头框(FOX)基因通过依赖于SHH - GLI通路、TGF - β通路等的转录调控参与胚胎发生,也通过基因扩增、逆转录病毒整合和染色体易位参与肿瘤发生。FOXN1、FOXN2(HTLF)、FOXN3(CHES1)和FOXN4构成FOXN家族。在此,我们通过生物信息学鉴定并表征了FOXN基因家族的一个新成员——FOXN5基因。IMAGE5167039(BC028191.1)是源自人类FOXN5基因的代表性cDNA。在大鼠基因组序列CH230 - 26K11(AC107575.5)中鉴定出由六个外显子组成的大鼠Foxn5基因。通过组装大鼠Foxn5外显子的核苷酸序列确定了大鼠Foxn5 cDNA的完整编码序列。人类FOXN5(292个氨基酸)和大鼠Foxn5(296个氨基酸)的总氨基酸同一性为77.4%。FOXN5的第173 - 254密码子为叉头结构域。由六个外显子组成的FOXN5基因在人类染色体11q23.3处与BCL9L基因相连。FOXN5是一个候选肿瘤抑制基因(TSG),就像11q23.1处的ARHGAP20(KIAA1391)、BTG4、SNF1LK2(SIK2)、DIXDC1(KIAA1735)基因,11q23.2处的TTC12(TPARM)基因,以及11q23.3处的IGSF4、DSCAML1、LL5A(PHLDB1)、BCL9L、RNF26和MFRP基因一样。这是关于人类FOXN5和大鼠Foxn5基因的首次报道。