Amplification of satellite III DNA in an unusually large chromosome 14p+ variant
- PMID: 2722196
- DOI: 10.1007/BF00284055
Amplification of satellite III DNA in an unusually large chromosome 14p+ variant
Abstract
A phenotypically normal male (WSm) was found to have an unusually large short arm of chromosome 14. Increase in the size of this variant chromosome [Wsm-var(14)] was estimated to be approximately 30% that of a normal chromosome 14 by G-banding using trypsin and staining with Leishman. The extra chromosomal material was positive in CBG staining (C-banding using BaOH and staining with Giemsa), suggesting the presence of repetitive DNA. In situ hybridisation using repetitive probes demonstrated this material to be strongly positive for satellite III DNA, and negative for Y-specific heterochromatic DNA. Hybridisation with an alpha DNA probe specific for human acrocentric chromosomes indicated the retention of the centromere, and the absence of alpha DNA in the extra chromosomal material. We propose the origin of the extra chromosomal material in WSm-var(14) to be a result of amplification of contiguous satellite III DNA that is normally present in the short arm of chromosome 14. This variant chromosome does not appear to be associated with the abnormal phenotype in WSm's daughter who is mentally retarded and carries a t(1;?)(q41;?) translocation of chromosome 1.
Similar articles
-
Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variant.Hum Genet. 1989 May;82(2):154-8. doi: 10.1007/BF00284049. Hum Genet. 1989. PMID: 2722191
-
Absence of satellite III DNA in the centromere and the proximal long-arm region of human chromosome 14: analysis of a 14p- variant.Cytogenet Cell Genet. 1992;61(1):78-80. doi: 10.1159/000133373. Cytogenet Cell Genet. 1992. PMID: 1505236
-
Coexistence of inverted Y, chromosome 15p+ and abnormal phenotype.Genet Couns. 1999;10(2):163-70. Genet Couns. 1999. PMID: 10422010 Review.
-
Breakpoints in Robertsonian translocations are localized to satellite III DNA by fluorescence in situ hybridization.Genomics. 1992 Dec;14(4):924-30. doi: 10.1016/s0888-7543(05)80113-2. Genomics. 1992. PMID: 1478673
-
Duplication of the short arm of the X chromosome in mother and daughter.Hum Genet. 1993 May;91(4):395-400. doi: 10.1007/BF00217366. Hum Genet. 1993. PMID: 8500796 Review.
Cited by
-
The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)].Hum Genet. 1991 Jun;87(2):173-6. doi: 10.1007/BF00204176. Hum Genet. 1991. PMID: 2066104
-
The Evolution of satellite III DNA subfamilies among primates.Am J Hum Genet. 2007 Mar;80(3):495-501. doi: 10.1086/512132. Epub 2007 Jan 23. Am J Hum Genet. 2007. PMID: 17273970 Free PMC article.
-
Identification and characterization of satellite III subfamilies to the acrocentric chromosomes.Chromosome Res. 2001;9(3):223-33. doi: 10.1023/a:1016648404388. Chromosome Res. 2001. PMID: 11330397
-
Amplification of (GACA)n simple repeats in an exceptional 14p+ marker chromosome.Hum Genet. 1994 Apr;93(4):375-82. doi: 10.1007/BF00201661. Hum Genet. 1994. PMID: 8168807
-
Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variant.Hum Genet. 1989 May;82(2):154-8. doi: 10.1007/BF00284049. Hum Genet. 1989. PMID: 2722191
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Research Materials
Miscellaneous