Choo K H, Earle E, Vissel B, Kalitsis P
Murdoch Institute for Research into Birth Defects, Royal Children's Hospital, Parkville, Australia.
Am J Hum Genet. 1992 Apr;50(4):706-16.
We describe a new subfamily of satellite III DNA (pTRS-63), which, by a combination of in situ hybridization to human metaphase chromosomes and analysis of a panel of somatic cell hybrids, is shown to be specific for human chromosome 14. This DNA has a basic 5-bp repeating unit of diverged GGAAT which is tandemly repeated and organized into either one of two distinct higher-order structures of 5 kb (designated the "L" form) or 4.8 kb (designated the "S" form). In addition, a third (Z) form, representing no detectable levels of this satellite III subfamily, is found. Results from five somatic cell hybrid lines and from a number of informative human individuals suggest that, on any one chromosome 14, only one of the three forms may exist. Subchromosomally, this sequence has been mapped to the p11 region and is distal to the domain occupied by another previously described satellite III subfamily (pTRS-47) found on chromosome 14. The pTRS-63 sequence described adds to the understanding of the structural organization of the short arm of human chromosome 14 and should be useful for the investigation of the molecular etiology of the frequently occurring t(13q14q) and t(14q21q) Robertsonian translocations.
我们描述了卫星III DNA的一个新亚家族(pTRS - 63),通过对人类中期染色体进行原位杂交以及对一组体细胞杂种进行分析,结果表明它对人类14号染色体具有特异性。这种DNA具有一个由发散的GGAAT组成的基本5碱基重复单元,该单元串联重复,并组织成两种不同的高阶结构之一,即5 kb(称为“L”型)或4.8 kb(称为“S”型)。此外,还发现了第三种(Z)型,其代表该卫星III亚家族的不可检测水平。来自五个体细胞杂种系和一些信息丰富的人类个体的结果表明,在任何一条14号染色体上,这三种形式中可能仅存在一种。在亚染色体水平上,该序列已定位到p11区域,并且位于14号染色体上另一个先前描述的卫星III亚家族(pTRS - 47)所占据区域的远端。所描述的pTRS - 63序列有助于增进对人类14号染色体短臂结构组织的理解,并且应该有助于研究频繁出现的t(13q14q)和t(14q21q)罗伯逊易位的分子病因。