Cloning and characterization of freac-9 (FKHL17), a novel kidney-expressed human forkhead gene that maps to chromosome 1p32-p34

被引:14
作者
Ernstsson, S
Betz, R
Lagercrantz, S
Larsson, C
Ericksson, S
Cederberg, A
Carlsson, P
Enerback, S
机构
[1] GOTHENBURG UNIV, DEPT MOL BIOL, LUNDBERG LAB, S-41390 GOTHENBURG, SWEDEN
[2] KAROLINSKA HOSP, ENDOCRINE TUMOR UNIV, DEPT MOL MED, S-17176 STOCKHOLM, SWEDEN
关键词
D O I
10.1006/geno.1997.4986
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We describe the cloning of a near full-length cDNA of 4258 nucleotides encoding freac-9 (HGMW-approved symbol FKHL17), a novel human forkhead gene, The 5 ' untranslated region is unusual since it is very long, 2127 nucleotides, and contains 15 upstream AUG codons, Hybridization to a panel consisting of RNA derived horn 50 different tissues showed that freac-9 is transcribed exclusively in the kidney, The kidney-derived cell lines COS-7 and 293 are shown to express freac-9. A combination of fluorescence in situ hybridization and somatic cell hybrids localizes freac-9 to the chromosomal region of 1p32-p34. The conceptual translation product predicts a protein of 372 amino acids with an N-terminal domain rich in acidic amino acids and with a high likelihood of forming an amphipatic helix, a DNA binding forkhead domain, and a C-terminal region that has a high probability of forming an amphipatic beta-sheet. The amino acid sequence of the DNA binding forkhead motif of FREAC-9 is identical to that of another forkhead protein, FREAC-4, whereas 12 substitutions are present at the nucleotide level. Ther-e are no similarities in regions outside of the DNA binding domains of FREAC-9 and FREAC-4 and since freac-4 maps to a different chromosome (5q12-q13) it is likely that sill evolutionary selection has acted to maintain identical DNA binding domains between these two kidney expressed transcription factors. (C) 1997 Academic Press.
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页码:78 / 85
页数:8
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