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人类CSF2和IL3基因的连锁图谱

Linkage mapping of the human CSF2 and IL3 genes.

作者信息

Frolova E I, Dolganov G M, Mazo I A, Smirnov D V, Copeland P, Stewart C, O'Brien S J, Dean M

机构信息

M.M. Shemyakin Institute of Bio-organic Chemistry, Academy of Sciences of the U.S.S.R., Moscow.

出版信息

Proc Natl Acad Sci U S A. 1991 Jun 1;88(11):4821-4. doi: 10.1073/pnas.88.11.4821.

Abstract

Interleukin 3 (encoded by the IL3 gene) and granulocyte-macrophage colony-stimulating factor (encoded by the CSF2 gene) are small secreted polypeptides that bind to specific cell surface receptors and regulate the growth, gene expression, and differentiation of many of the hematopoietic cell lineages, particularly nonlymphoid cells. The IL3 and CSF2 genes have been cloned and mapped to human chromosome bands 5q23-31. Only 10 kilobases of DNA separates the two genes, suggesting that they have a common origin and/or regulation. We have cloned 70 kilobases of genomic DNA that includes the IL3 and CSF2 genes, as well as flanking sequences, and report a physical map of this region. Several unique-sequence DNA segments have been identified in this region, and one of these fragments detects two restriction fragment length polymorphisms in DNA from unrelated Caucasians. Segregation of these DNA polymorphisms was followed in the Centre Etudé du Polymorphisme Humaine (CEPH) panel of 40 large three-generation pedigrees, and linkage was detected with 17 genetic markers previously typed in these families. Multipoint linkage analysis permits the placement of the region containing the IL3 and CSF2 structural genes on the recombination-genetic linkage map of chromosome 5q and thereby allows the role of these genes in leukemogenesis to be more critically examined.

摘要

白细胞介素3(由IL3基因编码)和粒细胞-巨噬细胞集落刺激因子(由CSF2基因编码)是小的分泌型多肽,它们与特定的细胞表面受体结合,并调节许多造血细胞谱系,特别是非淋巴细胞的生长、基因表达和分化。IL3和CSF2基因已被克隆并定位于人类染色体5q23 - 31带。两个基因之间仅相隔10千碱基的DNA,这表明它们有共同的起源和/或调控机制。我们克隆了包含IL3和CSF2基因以及侧翼序列的70千碱基的基因组DNA,并报告了该区域的物理图谱。在该区域已鉴定出几个单拷贝序列DNA片段,其中一个片段在无关的高加索人的DNA中检测到两种限制性片段长度多态性。在人类多态性研究中心(CEPH)的40个大型三代家系中追踪这些DNA多态性的分离情况,并检测到与这些家族中先前分型的17个遗传标记的连锁关系。多点连锁分析允许将包含IL3和CSF2结构基因的区域定位在5号染色体q臂的重组-遗传连锁图谱上,从而使这些基因在白血病发生中的作用能够得到更严格的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e67/51758/63a0b0946eb6/pnas01061-0268-a.jpg

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