Kostrzewa M, Müller U
Institut für Humangenetik, Justus-Liebig-Universität Giessen, Germany.
Mamm Genome. 1998 Feb;9(2):131-5. doi: 10.1007/s003359900703.
We report the genomic structure and entire sequence of the fibroblast growth factor receptor 4 (FGFR4) gene. The gene spans approximately 11.3 kb. It is composed of 18 exons ranging in size from 71 bp to 600 bp. Exon-intron boundaries follow the GT/AG rule. Exon 1 is untranslated and preceded by structural elements characteristic of a TATA-free promoter. Although there are promoter motifs in intron 4 as well, there is currently no evidence of alternative transcription of FGFR4. Comparison of exon-intron boundaries of FGFR4 with those of FGFR1 and 3 reveals a remarkable degree of homology. With the exception of four, exon boundaries are at identical positions in all three receptor genes. Short tandem repeat polymorphisms (STRPs) were identified in introns 2 and 16 of FGFR4. The STRPs together with the sequence information will facilitate the rapid analysis of FGFR4 in those human disorders in which this gene can be considered a candidate.
我们报道了成纤维细胞生长因子受体4(FGFR4)基因的基因组结构和完整序列。该基因跨度约为11.3 kb。它由18个外显子组成,大小从71 bp到600 bp不等。外显子-内含子边界遵循GT/AG规则。外显子1是非翻译的,其前面是无TATA框启动子的特征性结构元件。虽然内含子4中也有启动子基序,但目前尚无FGFR4存在可变转录的证据。将FGFR4的外显子-内含子边界与FGFR1和FGFR3的进行比较,发现它们具有高度的同源性。除了四个外显子边界外,所有三个受体基因的外显子边界位置相同。在FGFR4的内含子2和16中鉴定出短串联重复多态性(STRP)。这些STRP以及序列信息将有助于在那些可将该基因视为候选基因的人类疾病中快速分析FGFR4。