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HLA I类基因的端粒和着丝粒末端:YAC衍生黏粒的MCD图谱及740kb基因组DNA的序列分析

The telomeric and centromeric ends of HLA class I: MCD maps of YAC derived cosmids and sequence analysis of 740 kb of genomic DNA.

作者信息

Janer M, Guillaudeux T, Geraghty D, Geraghty D E

机构信息

Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle WA, USA.

出版信息

DNA Seq. 1996;7(1):33-8. doi: 10.3109/10425179609015644.

Abstract

We previously isolated and characterized a set of overlapping yeast artificial chromosome (YAC) clones spanning 2.4 Mb, including the entire MHC class I region, as a first step towards a detailed genetic analysis. We report here the genomic sequence of the two ends of HLA class I. The centromeric portion of HLA class I, extending from TNF to HLA-C was determined using two different sources of genomic DNA. As a first source, we sequenced cosmids (provided by T. Spies) derived from a total human DNA library which were mapped with conventional restriction digestion and fingerprinting. A second more generalizable approach was used to obtain cosmids for the remainder of the region. The new technology of Multiple-Complete-Digest (MCD) mapping, developed in Maynard Olson's laboratory, was used to map cosmids derived from YACs. This technique involves screening deep cosmid libraries derived from selected YACs and subjecting the cosmids to complete digestion with restriction enzymes, followed by computational assembly into completed maps. This method was also used to obtain material for sequence from three overlapping YACs covering a contiguous region from HLA-G to a point 330 kb telomeric. Among the plethora of new genetic information is a detailed picture of the organization of new multigene families contained within the telomeric end and of members of families spread throughout HLA class I. A clear relationship between the telomeric and centromeric ends of HLA class I has been defined, suggesting that large portions of these regions derived from a common ancestor. Our results demonstrate genomic sequencing to be one of the most effective and efficient means of identifying new genes, yielding information about genomic structure, regulation, and offering new insights into the meaning of physical relationships among functionally interacting genes.

摘要

我们先前分离并鉴定了一组重叠的酵母人工染色体(YAC)克隆,其跨度为2.4 Mb,包括整个MHC I类区域,作为迈向详细遗传分析的第一步。我们在此报告HLA I类两端的基因组序列。使用两种不同来源的基因组DNA确定了从TNF延伸至HLA - C的HLA I类着丝粒部分。作为第一个来源,我们对来自总人DNA文库的粘粒(由T. Spies提供)进行了测序,这些粘粒通过传统的限制性消化和指纹图谱进行定位。对于该区域的其余部分,采用了第二种更具通用性的方法来获取粘粒。在Maynard Olson实验室开发的多重完全消化(MCD)图谱新技术,用于对源自YAC的粘粒进行定位。该技术包括筛选源自选定YAC的深度粘粒文库,并用限制性酶对粘粒进行完全消化,随后通过计算组装成完整图谱。此方法还用于从三个重叠的YAC中获取用于测序的材料,这些YAC覆盖了从HLA - G到端粒方向330 kb连续区域。在大量新的遗传信息中,有端粒末端包含的新多基因家族以及遍布HLA I类的家族成员组织的详细图谱。已经明确了HLA I类端粒和着丝粒末端之间的清晰关系,表明这些区域的大部分源自共同祖先。我们的结果表明,基因组测序是鉴定新基因、产生有关基因组结构和调控信息以及为功能相互作用基因之间物理关系的意义提供新见解的最有效手段之一。

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