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采用不同染色技术和荧光原位杂交对欧洲扁蛎(双壳纲:扇贝科)染色体进行表征。

Characterization of Aequipecten opercularis (Bivalvia: Pectinidae) chromosomes by different staining techniques and fluorescent in situ hybridization.

作者信息

Insua A, López-Piñón M J, Méndez J

机构信息

Departamento de Biología Cellular y Molecular, Universidade da Coruña, A Zapateira, Spain.

出版信息

Genes Genet Syst. 1998 Aug;73(4):193-200. doi: 10.1266/ggs.73.193.

Abstract

The chromosomes of the queen scallop Aequipecten opercularis were studied using conventional Giemsa staining, chromosome measurements, C-banding, silver staining, and fluorescent in situ hybridization (FISH) with 18S-28S rDNA and 5S rDNA probes. The karyotype (2n = 26) consists of large metacentric (pairs 1 and 2), telocentric (pairs 3, 4, 5, 6, 7, 8, and 9), and small metacentric chromosomes (pairs 10, 11, 12, and 13). The C-bands observed can be described as major and minor C-bands which are differentiated according to the intensity of the fluorescence and the frequency of the detection. Major C-bands were found on the long arm of the chromosome pairs 6, 7, 8, and 9 in an intercalary or subterminal position. Minor C-bands were located in the centromeric region in all chromosomes of the complement and also on one arm of pairs 12 and 13 in a terminal position. Silver spots were detected on the telomere of the long arms of one or two chromosomes of pair 7 in every case, although in two individuals up to four additional silver spots were detected. These were located on pairs 8 and 9 in the same position as the C-bands. 18S-28S ribosomal genes were found by FISH on the long arm of chromosome pair 7.5S ribosomal genes were located subterminally on one arm of metacentric pair 1, but two sites were differentiated in the case of elongated chromosomes. The results obtained allow for the identification of at least six different chromosome pairs in A. opercularis and contribute to the construction of an idiogram that is suitable for gene mapping and establishing accurate interspecific comparisons in scallops.

摘要

采用常规吉姆萨染色、染色体测量、C带染色、银染以及用18S - 28S rDNA和5S rDNA探针进行荧光原位杂交(FISH)技术,对皇后扇贝(Aequipecten opercularis)的染色体进行了研究。其核型(2n = 26)由大型中着丝粒染色体(第1和2对)、端着丝粒染色体(第3、4、5、6、7、8和9对)以及小型中着丝粒染色体(第10、11、12和13对)组成。观察到的C带可分为主要C带和次要C带,它们根据荧光强度和检测频率进行区分。主要C带出现在第6、7、8和9对染色体长臂的居间或亚末端位置。次要C带位于所有互补染色体的着丝粒区域,也位于第12和13对染色体一条臂的末端位置。在每个样本中,在第7对染色体一条或两条染色体长臂的端粒上都检测到了银染点,不过在两个个体中还额外检测到了多达四个银染点,这些银染点位于第8和9对染色体上与C带相同的位置。通过FISH技术在第7对染色体长臂上发现了18S - 28S核糖体基因。5S核糖体基因位于中着丝粒第1对染色体一条臂的亚末端位置,但在染色体伸长的情况下可区分出两个位点。所获得的结果有助于识别皇后扇贝中至少六种不同的染色体对,并有助于构建适合基因定位以及在扇贝中进行准确种间比较的染色体模式图。

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