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一个以简单序列长度多态性为锚定的斑马鱼(Danio rerio)参考交叉DNA面板。

A reference cross DNA panel for zebrafish (Danio rerio) anchored with simple sequence length polymorphisms.

作者信息

Knapik E W, Goodman A, Atkinson O S, Roberts C T, Shiozawa M, Sim C U, Weksler-Zangen S, Trolliet M R, Futrell C, Innes B A, Koike G, McLaughlin M G, Pierre L, Simon J S, Vilallonga E, Roy M, Chiang P W, Fishman M C, Driever W, Jacob H J

机构信息

Cardiovascular Research Center, Massachusetts General Hospital, Charlestown 02129, USA.

出版信息

Development. 1996 Dec;123:451-60. doi: 10.1242/dev.123.1.451.

Abstract

The ultimate informativeness of the zebrafish mutations described in this issue will rest in part on the ability to clone these genes. However, the genetic infrastructure required for the positional cloning in zebrafish is still in its infancy. Here we report a reference cross panel of DNA, consisting of 520 F2 progeny (1040 meioses) that has been anchored to a zebrafish genetic linkage map by 102 simple sequence length polymorphisms. This reference cross DNA provides: (1) a panel of DNA from the cross that was used to construct the genetic linkage map, upon which polymorphic gene(s) and genetic markers can be mapped; (2) a fine order mapping tool, with a maximum resolution of 0.1 cM; and (3) a foundation for the development of a physical map (an ordered array of clones each containing a known portion of the genome). This reference cross DNA will serve as a resource enabling investigators to relate genes or genetic markers directly to a single genetic linkage map and avoid the problem of integrating different maps with different genetic markers, as must be currently done when using randomly amplified polymorphic DNA markers, or as has occurred with human genetic linkage maps.

摘要

本期所描述的斑马鱼突变的最终信息量将部分取决于克隆这些基因的能力。然而,斑马鱼中进行定位克隆所需的遗传基础设施仍处于起步阶段。在此,我们报告了一个DNA参考杂交群体,由520个F2后代(1040次减数分裂)组成,该群体已通过102个简单序列长度多态性锚定到斑马鱼遗传连锁图谱上。这个参考杂交DNA提供了:(1)用于构建遗传连锁图谱的杂交群体的DNA面板,多态基因和遗传标记可定位其上;(2)一个精细排序的定位工具,最大分辨率为0.1厘摩;以及(3)构建物理图谱(每个克隆包含基因组已知部分的有序阵列)的基础。这个参考杂交DNA将作为一种资源,使研究人员能够将基因或遗传标记直接与单个遗传连锁图谱相关联,避免整合具有不同遗传标记的不同图谱的问题,而这是目前使用随机扩增多态性DNA标记时必须做的,或者就像人类遗传连锁图谱那样已经出现的情况。

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