Allikmets R, Kashuba V I, Huebner K, LaForgia S, Kisselev L L, Klein G, Dean M, Zabarovsky E R
Laboratory of Viral Carcinogenesis, National Cancer Institute, Frederick, MD 21702-1201, USA. allikmet/fcrfv1.ncifcrf.gov
Chromosome Res. 1996 Jan;4(1):33-7. doi: 10.1007/BF02254942.
Twenty-two human chromosome 3 derived and partially sequenced Notl linking clones were mapped using two somatic cell hybrid panels. Somatic cell hybrid mapping was performed by Southern hybridization and/or by polymerase chain reaction (PCR), using 300-500 bp CpG-rich sequences surrounding Notl sites. Thus, 22 new Notl site-tagged (sequence tagged sites) STSs were created, distributed over the entire human chromosome 3. The majority of these linking clones tag known or unknown expressed sequences (genes). Together with other physical and genetic mapping methods, localization of Notl linking clones facilitates the construction of a long-range physical map and, at the same time, a transcriptional map of human chromosome 3.
使用两个体细胞杂交板对22个源自人类3号染色体且部分测序的Notl连接克隆进行了定位。通过Southern杂交和/或聚合酶链反应(PCR),利用Notl位点周围300 - 500 bp富含CpG的序列进行体细胞杂交定位。由此,创建了22个新的Notl位点标签(序列标签位点)STSs,它们分布在整个人类3号染色体上。这些连接克隆中的大多数标记了已知或未知的表达序列(基因)。与其他物理和遗传定位方法一起,Notl连接克隆的定位有助于构建人类3号染色体的长程物理图谱,同时也有助于构建转录图谱。