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首页> 外文期刊>Muscle and Nerve >Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.
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Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.

机译:鱼将250个粘粒和26个YAC克隆映射到4号染色体,并特别强调了4q35时的FSHD区。

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摘要

Facioscapulohumeral muscular dystrophy (FSHD) is located on chromosome 4q35, close to the telomere. FSHD patients carry deletions within a cluster of tandemly repeated DNA. Although expression of a functional FSHD gene will be altered in patients, the sequence itself may be unaffected by this deletion. Hence, the FSHD gene could lie outside of the deleted region. This study employs fluorescent in situ hybridization using chromosome 4-specific cosmid and YAC clones to rapidly saturate chromosome 4 with new markers. Some 250 cosmids and 26 YACs were regionally mapped, of which 5 YACs and 55 cosmids mapped to the distal portion of 4q. Only one of these clones (D4S1454) mapped telomerically to a translocation breakpoint specified by D4S187. Using two-color interphase mapping, the following marker order was obtained: Cen-D4S187-D4S1454-HSPCAL2-D4S163-D4S139-+ ++D4F35S1. Absence of additional markers mapping distal to D4F35S1 indicates that the linkage group containing the FSHD gene lies extremely close to the 4q telomere.
机译:面肩肱型肌营养不良症(FSHD)位于染色体4q35,靠近端粒。 FSHD患者在串联重复的DNA簇中携带缺失。尽管功能性FSHD基因的表达将在患者中发生改变,但序列本身可能不受此缺失的影响。因此,FSHD基因可能位于缺失区域之外。这项研究利用荧光原位杂交技术,使用4号染色体特异的粘粒和YAC克隆,用新标记快速饱和4号染色体。大约绘制了250个粘粒和26个YAC,其中5个YAC和55个粘粒被映射到4q的远端。这些克隆中只有一个(D4S1454)端粒化地映射到D4S187指定的易位断点。使用两色相间映射,可获得以下标记顺序:Cen-D4S187-D4S1454-HSPCAL2-D4S163-D4S139- + ++ D4F35S1。缺少位于D4F35S1远端的其他标记,表明包含FSHD基因的连接基团非常靠近4q端粒。

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