Please use this identifier to cite or link to this item:
|Scopus||Web of Science®||Altmetric|
|Title:||Physical localization of rRNA genes by two-colour fluorescent in-situ hybridization and sequence analysis of the 5s rRNA gene in Phalaris coerulescens|
|Citation:||Hereditas, 1997; 126(3):289-294|
|Xinmin Li, Rongqing Guo, Carsten Pederse, David Hayman, Peter Langridge|
|Abstract:||The 18S-5.8S-26S rDNA and 5s rDNA loci have been mapped physically by fluorescent in-situ hybridization to the chromosomes of Phalaris coerulescens. The biotin-labelled heterologous 18S-5.8S-26S rRNA probe (pTa71) detected one locus, which corresponded to the secondary constriction (nucleolar organizer) on the long arm of the satellited chromosome II. The homologous 5s rDNA probe (Bam2.12) detected two pairs of 5s rRNA gene clusters which were localized at two different non-satellited chromosomes, one near the telomere on the short arm of the chromosome I, which is the largest chromosome of the complement, and the other about 42 % out on the long arm of the chromosome III. A Bam HI fragment, containing the 5s rRNA gene, has been isolated and characterized. The 5s rDNA repeat unit is 309 bp in length, consisting of 121 bp highly conserved coding region and 188 bp variable spacer region. The karyotype of Phalaris coerulescens is characterized by the similar size of chromosomes within the group 2, group 3, or group 4. This study represents the first step towards the understanding the genome organization of Phalaris coerulescens and provides reliable markers for chromosome identification in this grass, an important species as a model system for the study of self-incompatibility in grasses.|
|Appears in Collections:||Genetics publications|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.