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人类集落刺激因子1(CSF1)基因重新定位于染色体1p13 - p21。

Reassignment of the human CSF1 gene to chromosome 1p13-p21.

作者信息

Morris S W, Valentine M B, Shapiro D N, Sublett J E, Deaven L L, Foust J T, Roberts W M, Cerretti D P, Look A T

机构信息

Department of Hematology-Oncology, St Jude Children's Research Hospital, Memphis, TN 38105.

出版信息

Blood. 1991 Oct 15;78(8):2013-20.

PMID:1912583
Abstract

Human macrophage colony-stimulating factor (CSF-1 or M-CSF) is encoded by a single gene that was previously assigned to the long arm of chromosome 5, band q33.1, in a region adjacent to the gene encoding its receptor (Pettenati MJ, et al, Proc Natl Acad Sci USA 84:2970, 1987). Using fluorescence in situ hybridization with genomic probes to examine normal metaphase chromosomes, we reassigned the human CSF1 gene to the short arm of chromosome 1, bands p13-p21. We confirmed this result by hybridizing a CSF1 cDNA probe to filters containing flow-sorted chromosomes and by identifying CSF1 sequences in DNAs extracted from human x rodent somatic cell hybrids that contained human chromosome 1 but not human chromosome 5. Our findings are consistent with studies that have shown tight linkage between the murine CSF1 and amylase genes, as part of a conserved linkage group between mouse chromosome 3 and the short arm of human chromosome 1, which also includes the genes encoding the beta subunits of thyrotropin and nerve growth factor. Assignment of the CSF1 gene to chromosome 1 at bands p13-p21 raises the possibility that it may be altered by certain nonrandom chromosomal abnormalities arising in human hematopoietic malignancies and solid tumors.

摘要

人巨噬细胞集落刺激因子(CSF-1或M-CSF)由单个基因编码,该基因先前被定位于5号染色体长臂q33.1带,位于编码其受体的基因附近区域(Pettenati MJ等人,《美国国家科学院院刊》84:2970,1987)。我们使用基因组探针进行荧光原位杂交来检测正常中期染色体,将人CSF1基因重新定位于1号染色体短臂p13-p21带。我们通过将CSF1 cDNA探针与包含流式分选染色体的滤膜杂交,并通过在从含有1号人类染色体但不含有5号人类染色体的人-啮齿动物体细胞杂种中提取的DNA中鉴定CSF1序列,证实了这一结果。我们的发现与一些研究一致,这些研究表明小鼠CSF1基因与淀粉酶基因紧密连锁,这是小鼠3号染色体与人类1号染色体短臂之间保守连锁群的一部分,该连锁群还包括编码促甲状腺激素β亚基和神经生长因子的基因。将CSF1基因定位于1号染色体p13-p21带增加了一种可能性,即它可能会被人类造血恶性肿瘤和实体瘤中出现的某些非随机染色体异常所改变。

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