Meyne J, Goodwin E H, Moyzis R K
Life Sciences Division, Los Alamos National Laboratory, NM 87545.
Chromosoma. 1994 Apr;103(2):99-103. doi: 10.1007/BF00352318.
The predominant chromosomal locations of human satellite I DNA were detected using fluorescent in situ hybridization (FISH). Synthetic deoxyoligonucleotides designed from consensus sequences of the simple sequence repeats of satellite 1 were used as probes. The most abundant satellite I repeat, the -A-B-A-B-A- form, is located at the pericentromeric regions of chromosomes 3, 4, 13, 14, 15, 21, and 22. The less abundant -B-B-B-form was not detected on chromosome 4, but was present at all the other locations. A variation of FISH that allows strand-specific hybridization of single-stranded probes (CO-FISH) determined that the human satellite I sequences are predominantly arranged in head-to-tail fashion along the DNA strand.
利用荧光原位杂交(FISH)技术检测了人类卫星I DNA在染色体上的主要定位。根据卫星1简单序列重复的共有序列设计的合成脱氧寡核苷酸用作探针。最丰富的卫星I重复序列,即-A-B-A-B-A-形式,位于3号、4号、13号、14号、15号、21号和22号染色体的着丝粒周围区域。含量较少的-B-B-B-形式在4号染色体上未检测到,但在所有其他位置均有出现。一种允许单链探针进行链特异性杂交的FISH变体(CO-FISH)确定,人类卫星I序列主要沿DNA链以头对头的方式排列。