Dore E, Pace T, Ponzi M, Scotti R, Frontali C
Mol Biochem Parasitol. 1986 Nov;21(2):121-7. doi: 10.1016/0166-6851(86)90015-0.
The telomeric sequence cloned from Plasmodium berghei (see M. Ponzi et al. (1985) EMBO J. 4, 2991-2995) was tested for species specificity. A telomeric and a subtelomeric fragment of the cloned insert served as separate, labelled probes on pulsed field gradient electrophoretical patterns and on genomic digests from the rodent malarias Plasmodium yoelii, Plasmodium chabaudi and from the human malaria Plasmodium falciparum. Results indicate that the subtelomeric fragment, abundantly represented in two chromosomes of P. berghei, is not present in the other DNA tested, while the telomeric fragment is present in every chromosome-sized molecule in all the species tested. The telomeric location in the other genomes of the sequences homologous to the P. berghei telomeric probe is confirmed by experiments with Bal 31 exonuclease. In all cases, the TaqI site appears to delimit the common telomeric portion.
对从伯氏疟原虫克隆的端粒序列(见M. Ponzi等人,(1985年)《欧洲分子生物学组织杂志》4,2991 - 2995)进行了物种特异性测试。克隆插入片段的一个端粒片段和一个亚端粒片段分别作为标记探针,用于脉冲场梯度电泳图谱以及来自啮齿动物疟原虫约氏疟原虫、查巴迪疟原虫和人类疟原虫恶性疟原虫的基因组消化产物。结果表明,在伯氏疟原虫两条染色体中大量存在的亚端粒片段,在所测试的其他DNA中不存在,而端粒片段存在于所有测试物种的每个染色体大小的分子中。通过用Bal 31核酸外切酶进行的实验,证实了与伯氏疟原虫端粒探针同源的序列在其他基因组中的端粒位置。在所有情况下,TaqI位点似乎界定了共同的端粒部分。