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日本盲鳗(Eptatretus okinoseanus)中生殖系限制的高度重复DNA序列及其染色体定位

Germ line-restricted, highly repeated DNA sequences and their chromosomal localization in a Japanese hagfish (Eptatretus okinoseanus).

作者信息

Kubota S, Kuro-o M, Mizuno S, Kohno S

机构信息

Department of Biology, Faculty of Science, Toho University, Chiba, Japan.

出版信息

Chromosoma. 1993 Feb;102(3):163-73. doi: 10.1007/BF00387731.

DOI:10.1007/BF00387731
PMID:8458254
Abstract

The various species of Japanese hagfish, namely, Eptatretus okinoseanus (types A and B), Eptatretus burgeri and Myxine garmani, are known to eliminate a fraction of their chromosomes during early embryogenesis. High molecular weight DNA from germ line cells and somatic cells of these hagfish species was isolated and digested with different restriction enzymes. The DNA fragments were separated by agarose gel electrophoresis. Digestion with BamHI and DraI generated two weak bands and one weak band, respectively, that were estimated to be about 90, and 180 bp and about 90 bp long and were limited to the germ line DNA in both types of E. okinoseanus. DNA filter hybridization experiments showed that the two BamHI fragments and the one DraI fragment were present almost exclusively in the germ line DNA of E. okinoseanus. Thus, these DNA fragments appear to be eliminated during embryogenesis. Moreover, evidence was obtained that these fragments are highly and tandemly repeated. Molecular cloning and sequence analysis revealed that the BamHI fragments are mainly composed of a family of closely related sequences that are 95 bp long (EEEo1, for Eliminated Element of E. okinoseanus 1), and the DraI fragment is composed of another family of closely related sequences that are 85 bp long (EEEo2). The two DNA families account for about 19% of the total eliminated DNA in E. okinoseanus type A. Fluorescence in situ hybridization experiments demonstrated that the two families of DNA are located on several C-band-positive, small chromosomes that are limited to germ cells in both types of E. okinoseanus.

摘要

已知日本盲鳗的各个物种,即冲绳盲鳗(A 型和 B 型)、蒲氏黏盲鳗和格氏黏盲鳗,在胚胎发育早期会消除一部分染色体。从这些盲鳗物种的生殖细胞和体细胞中分离出高分子量 DNA,并用不同的限制酶进行消化。DNA 片段通过琼脂糖凝胶电泳分离。用 BamHI 和 DraI 消化分别产生了两条弱带和一条弱带,估计长度分别约为 90 和 180 碱基对以及约 90 碱基对,并且仅限于两种冲绳盲鳗的生殖系 DNA。DNA 滤膜杂交实验表明,这两个 BamHI 片段和一个 DraI 片段几乎只存在于冲绳盲鳗的生殖系 DNA 中。因此,这些 DNA 片段似乎在胚胎发育过程中被消除。此外,有证据表明这些片段是高度串联重复的。分子克隆和序列分析表明,BamHI 片段主要由一个长度为 95 碱基对的密切相关序列家族组成(EEEo1,即冲绳盲鳗消除元件 1),而 DraI 片段由另一个长度为 85 碱基对的密切相关序列家族组成(EEEo2)。这两个 DNA 家族约占 A 型冲绳盲鳗总消除 DNA 的 19%。荧光原位杂交实验表明,这两个 DNA 家族位于几个 C 带阳性的小染色体上,这些染色体仅限于两种冲绳盲鳗的生殖细胞。

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