Shi Q, Shan X, Zhang J, Zhang X, Chen Y, Deng X, Huang H, Yu L, Zhao S, Zheng Q, Adler I
Department of Biology, Nanjing Normal University, Nanjing, Jiangsu, 210097 P. R. China.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 1999 Feb 10;16(1):36-40.
To prepare DNA probe which can be used to accurately detect chromosome 21 copy number in human interphase nuclei by fluorescence in situ hybridization (FISH).
A probe was produced by universal primer PCR from YAC clone 881D2 and characterized by FISH to metaphases and interphase nuclei of peripheral lymphocytes from 8 normal individuals and 5 patients suffering from trisomy 21.
A DNA probe was produced and its characteristics were :(1) Most of the probes ranged in size from 350bp to 750bp; (2) The hybridization signals of the probes were located near centromere on long arm of human chromosome 21; (3) In 1524 metaphases scored, about 99.95% of hybridization signals were located on chromosome 21; (4) The signals were very bright and recognizable easily in both metaphases and interphases nuclei; (5) The expected copy number of chromosome 21 was detected by FISH with the probe in more than 98.40% of interphase nuclei and 99.60% of metaphases.
The DNA probe reported here is suitable for the detection of chromosome 21 copy number in interphase nuclei and for the study of segregation of chromosome 21 during mitoses of human lymphocytes in culture.
制备可用于通过荧光原位杂交(FISH)准确检测人间期核中21号染色体拷贝数的DNA探针。
用通用引物PCR从YAC克隆881D2制备探针,并用FISH对8名正常个体和5名21三体综合征患者外周血淋巴细胞的中期和间期核进行鉴定。
制备了一种DNA探针,其特点为:(1)大多数探针大小在350bp至750bp之间;(2)探针的杂交信号位于人21号染色体长臂的着丝粒附近;(3)在计数的1524个中期相中,约99.95%的杂交信号位于21号染色体上;(4)信号在中期相和间期核中都非常明亮且易于识别;(5)用该探针通过FISH在超过98.40%的间期核和99.60%的中期相中检测到了预期的21号染色体拷贝数。
本文报道的DNA探针适用于检测间期核中21号染色体的拷贝数以及研究培养的人淋巴细胞有丝分裂过程中21号染色体的分离情况。