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人类15号染色体异常G组样染色体的优先衍生

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15.

作者信息

Schreck R R, Breg W R, Erlanger B F, Miller O J

出版信息

Hum Genet. 1977 Apr 7;36(1):1-12. doi: 10.1007/BF00390430.

Abstract

The marked binding of antibodies specific for 5-methylcytidine to the short arm of chromosome 15 distinguishes this chromosome from the other human acrocentrics. This method has been used to study over 60 individuals including 12 who did not have Down's syndrome, but who did have an extra G-group sized acrocentric chromosome. In six cases the extra chromosome did not show intensive binding of anti-5-methylcytidine. In the other six cases, the extra chromosome contained a 5-methylcytidine rich band at each end indicating that both ends were derived from chromosome 15 and contained centromeric heterochromatin normally present on the short arm of chromosome 15. The duplication of short arm material in the abnormal chromosomes was confirmed in all cases by quinacrine staining, nucleolar organizer (Ag-AS) staining or C-banding. In three cases, the abnormal chromosome appeared to arise from two different chromosomes 15. Several possible mechanisms for the production of the abnormal chromosome are discussed. The individuals with this abnormal chromosome all showed some degree of mental retardation, but few common physical findings.

摘要

对5-甲基胞嘧啶具有特异性的抗体与15号染色体短臂的显著结合,使得这条染色体有别于其他人类近端着丝粒染色体。该方法已用于研究60多名个体,其中包括12名没有唐氏综合征但有一条额外的G组大小近端着丝粒染色体的个体。在6例中,额外的染色体未显示抗5-甲基胞嘧啶的强烈结合。在其他6例中,额外的染色体两端各有一条富含5-甲基胞嘧啶的带,表明两端均来自15号染色体,且含有通常存在于15号染色体短臂上的着丝粒异染色质。在所有病例中,通过喹吖因染色、核仁组织区(Ag-AS)染色或C带染色证实了异常染色体上短臂物质的重复。在3例中,异常染色体似乎源自两条不同的15号染色体。文中讨论了产生异常染色体的几种可能机制。具有这种异常染色体的个体均表现出一定程度的智力迟钝,但几乎没有共同的体格检查发现。

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