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包含人类FGF1基因完整转录单位的酵母人工染色体的分离:跨越人类染色体5q31.3→q32的一个720 kb重叠群。

Isolation of yeast artificial chromosomes containing the entire transcriptional unit of the human FGF1 gene: a 720-kb contig spanning human chromosome 5q31.3-->q32.

作者信息

Chiu I M, Liu Y, Payson R A

机构信息

Department of Internal Medicine, Ohio State University, Columbus 43210, USA.

出版信息

Cancer Genet Cytogenet. 1998 Oct 1;106(1):1-10. doi: 10.1016/s0165-4608(98)00031-4.

Abstract

The q31-q33 region of chromosome 5 includes a number of genes encoding growth factors, growth factor receptors, and hormone/neurotransmitter receptors. The human fibroblast growth factor 1 locus (FGF1) resides in this region of chromosome 5, which is frequently lost in myelodysplastic syndromes and acute myeloid leukemia patients. Other disease loci, including the loci for limb-girdle muscular dystrophy and an autosomal dominant deafness, have been mapped on this region, but their genes have not been isolated. It was shown that the critical region lost in two patients with the 5q- syndrome resides between FGF1 and IL12B. We previously reported the construction of a yeast artificial chromosome (YAC) contig spanning 330 kb around the FGF1 gene. Here we report the isolation of additional YAC clones that extend 290 kb from the previous contig. Sequence-tagged sites developed from the outermost YAC ends were utilized in the contig cloning of two P1 clones P1Y2 and P1Y8. Together, these YAC and P1 clones span 720 kb around the FGF1 locus. With the use of fluorescence in situ hybridization, a physical map has been constructed of these P1 and GRL (glucocorticoid receptor locus) probes on metaphase and interphase chromosomes. On the basis of our work and the known orientation of GRL transcription, the determined order of these loci on chromosome 5q31.3-q32 is centromere-P1Y8-3'[FGF1]5'-P1Y2-5'[GRL]3'-telome re. Knowing the transcriptional orientation of the FGF1 gene relative to the centromere will now facilitate the directional cloning of clinically important genes that may reside in this region.

摘要

5号染色体的q31-q33区域包含许多编码生长因子、生长因子受体以及激素/神经递质受体的基因。人类成纤维细胞生长因子1基因座(FGF1)位于5号染色体的这一区域,在骨髓增生异常综合征和急性髓系白血病患者中该区域常发生缺失。其他疾病基因座,包括肢带型肌营养不良和常染色体显性遗传性耳聋的基因座,也已定位在该区域,但它们的基因尚未分离出来。研究表明,两名患有5q-综合征的患者中缺失的关键区域位于FGF1和IL12B之间。我们之前报道了构建一个围绕FGF1基因、跨度为330 kb的酵母人工染色体(YAC)重叠群。在此,我们报告分离出了另外一些YAC克隆,它们从先前的重叠群延伸了290 kb。从最外侧的YAC末端开发的序列标签位点被用于两个P1克隆P1Y2和P1Y8的重叠群克隆。这些YAC和P1克隆共同围绕FGF1基因座跨越了720 kb。通过荧光原位杂交技术,已构建出这些P1和糖皮质激素受体基因座(GRL)探针在中期和间期染色体上的物理图谱。基于我们的工作以及GRL转录的已知方向,确定这些基因座在5号染色体q31.3-q32上的顺序为着丝粒-P1Y8-3'[FGF1]5'-P1Y2-5'[GRL]3'-端粒。了解FGF1基因相对于着丝粒的转录方向,将有助于定向克隆可能位于该区域的临床重要基因。

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