Islam-Faridi M Nurul, Nelson C Dana, Kubisiak Thomas L
Forest Tree Molecular Cytogenetics Laboratory, Southern Institute of Forest Genetics, Southern Research Station, USDA Forest Service, Texas A&M University, 2585-TAMU, College Station, TX 77843-2585, USA.
Genome. 2007 Feb;50(2):241-51. doi: 10.1139/g06-153.
A reference karyotype is presented for loblolly pine (Pinus taeda L., subgenus Pinus, section Pinus, subsection Australes), based on fluorescent in situ hybridization (FISH), using 18S-28S rDNA, 5S rDNA, and an Arabidopsis-type telomere repeat sequence (A-type TRS). Well separated somatic chromosomes were prepared from colchicine-treated root meristems, using an enzymatic digestion technique. Statistical analyses performed on chromosome-arm lengths, centromeric indices, and interstitial rDNA and telomeric positions were based on observations from 6 well-separated metaphase cells from each of 3 unrelated trees. Statistically, 7 of the 12 loblolly pine chromosomes could be distinguished by their relative lengths. Centromeric indices were unable to distinguish additional chromosomes. However, the position and relative strength of the rDNA and telomeric sites made it possible to uniquely identify all of the chromosomes, providing a reference karyotype for use in comparative genome analyses. A dichotomous key was developed to aid in the identification of loblolly pine chromosomes and their comparison to chromosomes of other Pinus spp. A cytomolecular map was developed using the interstitial 18S-28S rDNA and A-type TRS signals. A total of 54 bins were assigned, ranging from 3 to 5 bins per chromosome. This is the first report of a chromosome-anchored physical map for a conifer that includes a dichotomous key for accurate and consistent identification of the P. taeda chromosomes.
基于荧光原位杂交(FISH)技术,利用18S - 28S核糖体DNA(rDNA)、5S rDNA和拟南芥型端粒重复序列(A - 型TRS),构建了火炬松(Pinus taeda L.,松属,松亚属,松组,南方松亚组)的参考核型。采用酶解技术,从经秋水仙碱处理的根尖分生组织中制备出分离良好的体细胞染色体。对染色体臂长度、着丝粒指数以及居间rDNA和端粒位置进行的统计分析,基于对3棵不相关树木中每棵树的6个分离良好的中期细胞的观察。从统计学角度看,火炬松的12条染色体中有7条可通过其相对长度加以区分。着丝粒指数无法区分其他染色体。然而,rDNA和端粒位点的位置及相对强度使得能够唯一识别所有染色体,从而提供了一个用于比较基因组分析的参考核型。开发了一个双歧检索表,以帮助识别火炬松染色体并将其与其他松属物种的染色体进行比较。利用居间18S - 28S rDNA和A - 型TRS信号构建了细胞分子图谱。总共划分了54个区间,每条染色体有3至5个区间。这是关于针叶树染色体锚定物理图谱的首篇报道,其中包括用于准确一致地识别火炬松染色体的双歧检索表。