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通过荧光原位杂交进行核型分析和基因定位后,将连锁群分配到豌豆染色体上。

Assignment of linkage groups to pea chromosomes after karyotyping and gene mapping by fluorescent in situ hybridization.

作者信息

Fuchs J, Kühne M, Schubert I

机构信息

Institut für Pflanzengenetik und Kulturpflanzenforschung (IPK), D-06466 Gatersleben, Germany.

出版信息

Chromosoma. 1998 Sep;107(4):272-6. doi: 10.1007/s004120050308.

Abstract

Chromosomes of the pea (Pisum sativum L.) were submitted to fluorescent in situ hybridization (FISH) with probes specific for the oligonucleotides (AG)12, (AC)12, (GAA)10, and (GATA)7 and for the genes encoding 25S rRNA, 5S rRNA and the storage proteins legumin A, K and vicilin. A fourth 5S rRNA gene locus, apparently specific for an accession of the cultivar Grüne Victoria, was newly detected. This allowed all seven chromosome pairs to be distinguished by FISH signals of rRNA genes. The same was possible using a combination of oligonucleotide probes or of oligonucleotides and rRNA gene-specific probes in multicolour FISH. Rehybridization with the 5S rRNA gene-specific probe allowed us to assign vicilin genes to the short arm of chromosome 5, the single legumin A locus to the long arm of chromosome 3 and the legumin B-type genes (exemplified by legumin K) to one locus on the short arm of chromosome 6. Correlation of these data with an updated version of the pea genetic map allowed the assignment of most linkage groups to defined chromosomes. It only remains to be established which of linkage groups IV and VII corresponds to the satellited chromosomes 4 or 7, respectively.

摘要

将豌豆(Pisum sativum L.)的染色体与针对寡核苷酸(AG)12、(AC)12、(GAA)10和(GATA)7以及编码25S rRNA、5S rRNA和贮藏蛋白豆球蛋白A、K和豌豆球蛋白的基因的探针进行荧光原位杂交(FISH)。新检测到了一个显然是栽培品种Grüne Victoria的一个变种所特有的第四个5S rRNA基因位点。这使得所有七对染色体都能通过rRNA基因的FISH信号加以区分。使用寡核苷酸探针或寡核苷酸与rRNA基因特异性探针的组合进行多色FISH也能做到这一点。用5S rRNA基因特异性探针重新杂交使我们能够将豌豆球蛋白基因定位到5号染色体的短臂上,将单个豆球蛋白A位点定位到3号染色体的长臂上,并将豆球蛋白B型基因(以豆球蛋白K为例)定位到6号染色体短臂上的一个位点。将这些数据与豌豆遗传图谱的更新版本进行关联,使得大多数连锁群能够定位到特定的染色体上。只剩下确定连锁群IV和VII中的哪一个分别对应于具随体的4号或7号染色体。

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