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Characterization of AFLP sequences from regions of maize B chromosome defined by 12 B-10L translocations

机译:Characterization of aFLp sequences from regions of maize B chromosome defined by 12 B-10L translocations

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摘要

Maize B chromosome sequences have been previously cloned by microdissection, and all are proven to be highly repetitive, to be homologous to the normal complement, and to show no similarity to any published gene other than mobile elements. In this study, we isolated sequences from defined B regions. The strategy involved identification and then mapping of AFLP-derived B fragments before cloning. Of 14 B AFLPs, 13 were mapped by 12 B-10L translocations: 3 around the centromeric knob region, 3 in the proximal euchromatic, I around the border of proximal euchromatic and distal heterochromatic, and 6 in the distal heterochromatic region of the B long arm. The AFLP fragments were cloned and sequenced. Analogous to the microdissected sequences, all sequences were repetitive, and all but two were highly homologous to the A chromosomes. FISH signals of all but three clones appeared in pachytene B as well as in somatic A and B chromosomes. None of these clones exhibits identity to any published gene. Six clones displayed homology to two centromeric BACs, four to sequences of chromosomes 3, 4, 7, and 10, four to retrotransposons, and three to no sequence deposited in GenBank. Furthermore, flanking regions of two highly B-specific clones were characterized, showing extension of a B-exclusive nature. The possibility of the presence of novel B repeat(s) is discussed.
机译:玉米B染色体序列先前已通过显微切割法克隆,并且全部被证明具有高度重复性,与正常补体同源,并且与除可移动元件外的任何已发表基因均无相似性。在这项研究中,我们从定义的B区中分离了序列。该策略涉及克隆前识别和定位来自AFLP的B片段。在14个B AFLP中,有13个通过12个B-10L易位进行定位:3个围绕着着丝粒结区,3个位于近端常色中,I围绕了近端常色和远侧异色的边界,6个位于远侧B的异色区域臂。克隆AFLP片段并测序。类似于显微切割的序列,所有序列都是重复的,除了两个以外,所有序列都与A染色体高度同源。除三个克隆外,其余所有克隆的FISH信号均出现在粗线期B以及体细胞A和B染色体中。这些克隆都没有表现出与任何已公开基因的同一性。六个克隆显示与两个着丝粒BAC同源,四个与染色体3、4、7和10染色体序列同源,四个与逆转座子同源,三个与GenBank中没有序列同源。此外,表征了两个高度B特异性克隆的侧翼区域,显示了B排他性的延伸。讨论了新的B重复存在的可能性。

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    Peng S.F.; Lin Y.P.; Lin B.Y.;

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  • 年度 2014
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