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拟步甲Misolampus goudoti异染色质的特征:两个卫星DNA家族的克隆及用限制酶对染色体的消化

Characterization of the heterochromatin of the darkling beetle Misolampus goudoti: cloning of two satellite DNA families and digestion of chromosomes with restriction enzymes.

作者信息

Pons J, Petitpierre E, Juan C

机构信息

Departament de Biologia Ambiental, Universitat de les Illes Balears, Palma de Mallorca, Spain.

出版信息

Hereditas. 1993;119(2):179-85. doi: 10.1111/j.1601-5223.1993.00179.x.

DOI:10.1111/j.1601-5223.1993.00179.x
PMID:8106263
Abstract

The darkling beetle Misolampus goudoti Er. has 58% of C-banded chromosome material. In this paper we deal with the study of the heterochromatin of this insect both by molecular and cytogenetical methods. Two different satellite DNA families have been characterized in Misolampus goudoti by agarose gel electrophoresis of EcoRI and PstI restriction fragments, respectively. The EcoRI family is composed of a monomeric unit of 196 bp (64.3% A-T rich) DNA sequence, representing about 120,000 copies per haploid genome. The presence of frequent intermediate-size satellite variants and an internal direct repetition of 61 bp in the EcoRI repetitive main monomer suggest that the evolution of this satellite proceeded by unequal crossing-over, occurring both within and between the 196 bp unit. Another highly repetitive sequence, defined by digestion of genomic DNA with PstI, has a more complex unit of 1.2 kb with about 70,000 copies per haploid genome. In situ digestion of M. goudoti chromosomes with restriction enzymes shows a non-specific chromosome DNA extraction from pericentromeric positions with EcoRI and chromosome specific extraction of DNA with PstI and HinfI. This is discussed in relation to the chromosomal location of both satellites.

摘要

暗黑甲虫米索兰普斯古多蒂(Misolampus goudoti Er.)有58%的C带染色体物质。在本文中,我们通过分子和细胞遗传学方法对这种昆虫的异染色质进行了研究。分别通过对EcoRI和PstI限制性片段进行琼脂糖凝胶电泳,在米索兰普斯古多蒂中鉴定出了两个不同的卫星DNA家族。EcoRI家族由一个196 bp(富含64.3% A-T)的DNA序列单体单元组成,每个单倍体基因组约有120,000个拷贝。EcoRI重复主单体中频繁出现中等大小的卫星变体以及61 bp的内部直接重复,这表明该卫星的进化是通过不等交换进行的,这种交换发生在196 bp单元内部和之间。另一个高度重复序列,通过用PstI消化基因组DNA来定义,其单元更为复杂,为1.2 kb,每个单倍体基因组约有70,000个拷贝。用限制性酶对米索兰普斯古多蒂染色体进行原位消化显示,用EcoRI从着丝粒周围位置进行非特异性染色体DNA提取,用PstI和HinfI进行染色体特异性DNA提取。这与两种卫星在染色体上的定位有关进行了讨论。

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