Jücker M, Roebroek A J, Mautner J, Koch K, Eick D, Diehl V, Van de Ven W J, Tesch H
I. Medizinische Klinik, Universität Köln, Germany.
Oncogene. 1992 May;7(5):943-52.
The human c-fps/fes proto-oncogene is expressed as a transcript of about 3.0 kb in both normal and leukemic myeloid cells. We have detected truncated c-fps/fes transcripts of about 0.9 kb in a panel of human lymphoma and lymphoid leukemia cell lines, but not in normal untransformed hematopoietic cells. Analysis of the chromatin structure of the c-fps/fes gene revealed DNAase I-hypersensitive sites in the 5' region of the gene and in exon 16. The presence and absence of these sites correlates with the expression of the 3.0 kb and 0.9 kb c-fps/fes RNAs respectively. The truncated transcripts initiate at two distinct sites within exon 16 of the c-fps/fes gene. The genomic region 5' to the transcription initiation sites is G+C rich but does not contain typical promoter consensus sequences. Sequence analysis of a cDNA clone of the truncated c-fps/fes transcripts did not reveal any point mutation and the truncated transcripts are normally spliced using the regular splice donor and acceptor sites. A putative open reading frame encompasses the phosphotransfer motif and the autophosphorylation site of the fps/fes kinase domain. In vitro transcription/translation of a cDNA clone corresponding to the truncated c-fps/fes transcripts revealed a protein of 17 kDa. There are no translocations or rearrangements in or around the c-fps/fes gene in cell lines which express the truncated c-fps/fes transcripts. This alternative transcription of c-fps/fes may indicate a novel activation process of this proto-oncogene.
人类c-fps/fes原癌基因在正常和白血病髓系细胞中均表达为约3.0 kb的转录本。我们在一组人类淋巴瘤和淋巴细胞白血病细胞系中检测到约0.9 kb的截短型c-fps/fes转录本,但在正常未转化的造血细胞中未检测到。对c-fps/fes基因染色质结构的分析揭示了该基因5'区域和外显子16中的DNA酶I超敏位点。这些位点的存在与否分别与3.0 kb和0.9 kb的c-fps/fes RNA的表达相关。截短的转录本在c-fps/fes基因外显子16内的两个不同位点起始。转录起始位点5'端的基因组区域富含G+C,但不包含典型的启动子共有序列。对截短的c-fps/fes转录本的cDNA克隆进行序列分析未发现任何点突变,并且截短的转录本使用常规的剪接供体和受体位点进行正常剪接。一个推定的开放阅读框包含fps/fes激酶结构域的磷酸转移基序和自磷酸化位点。对与截短的c-fps/fes转录本对应的cDNA克隆进行体外转录/翻译,揭示了一种17 kDa的蛋白质。在表达截短的c-fps/fes转录本的细胞系中,c-fps/fes基因内部或周围没有易位或重排。c-fps/fes的这种选择性转录可能表明该原癌基因的一种新的激活过程。