Genomic in situ hybridization in interspecific hybrids of scallops (Bivalvia, Pectinidae) and localization of the satellite DNA Cf303, and the vertebrate telomeric sequences (TTAGGG)n on chromosomes of scallop Chlamys farreri (Jones & Preston, 1904)

被引:1
作者
Hu, Liping [1 ,2 ]
Jiang, Liming [1 ]
Bi, Ke [3 ]
Liao, Huan [1 ]
Yang, Zujing [1 ]
Huang, Xiaoting [1 ]
Bao, Zhenmin [1 ,4 ]
机构
[1] Ocean Univ China, Coll Marine Life Sci, Minist Educ, Key Lab Marine Genet & Breeding, 5 Yushan Rd, Qingdao 266003, Peoples R China
[2] Yantai Fisheries Res Inst, Yantai 264003, Peoples R China
[3] Univ Calif Berkeley, Museum Vertebrate Zool, Berkeley, CA 94720 USA
[4] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Fisheries Sci & Food Prod Proc, Qingdao, Peoples R China
基金
中国国家自然科学基金;
关键词
GISH banding; FISH; Cf303; telomere; scallop; CYTOGENETIC CHARACTERIZATION; REPETITIVE DNA; DONAX-TRUNCULUS; PACIFIC OYSTER; ARGOPECTEN-IRRADIANS; AEGILOPS-SPELTOIDES; STAINING TECHNIQUES; PARENTAL GENOMES; RIBOSOMAL DNA; EVOLUTION;
D O I
10.3897/CompCytogen.v12i1.14995
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Mitotic chromosome preparations of the interspecific hybrids Chlamys farreri (Jones & Preston, 1904) x Patinopecten yessoensis (Jay, 1857), C. farreri x Argopecten irradinas (Lamarck, 1819) and C. farreri x Mimachlamys nobilis (Reeve, 1852) were used to compare two different scallop genomes in a single slide. Although genomic in situ hybridization (GISH) using genomic DNA from each scallop species as probe painted mitotic chromosomes of the interspecific hybrids, the painting results were not uniform; instead it showed species-specific distribution patterns of fluorescent signals among the chromosomes. The most prominent GISH-bands were mainly located at centromeric or telomeric regions of scallop chromosomes. In order to illustrate the sequence constitution of the GISH-bands, the satellite Cf303 sequences of C. farreri and the vertebrate telomeric (TTAGGG)(n) sequences were used to map mitotic chromosomes
引用
收藏
页码:83 / 95
页数:13
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