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玉米 Bz-M2(ac) 等位基因 Ac 元件的转座模式。

Transposition Pattern of the Maize Element Ac from the Bz-M2(ac) Allele.

机构信息

Advanced Genetic Sciences, 6701 San Pablo Avenue, Oakland, California 94608.

出版信息

Genetics. 1989 Jun;122(2):447-57. doi: 10.1093/genetics/122.2.447.

Abstract

The pattern of transposition of Ac from the mutable allele bz-m2(Ac) has been investigated. Stable (bz-s) and finely spotted (bz-m(F)) exceptions were selected from coarsely spotted bz-m2(Ac) ears. The presence or absence of a transposed Ac (trAc) in the genome was determined and, when present, the location of the trAc was mapped relative to the flanking markers sh and wx. The salient general features of Ac transposition to sites linked to bz are that the receptor sites tend to be clustered on either side of the bz donor site and that transposition is bidirectional and nonpolar. Thus, the symmetrical clustering in the distribution of receptor sites adjacent to bz differs from the asymmetrical clustering reported in 1984 for the P locus by I. M. GREENBLATT. Though Ac tends to transpose preferentially to closely linked sites, an appreciable fraction of Ac transpositions from bz-m2(Ac) is to unlinked sites: 41% among bz-s derivatives and 59% among bz-m(F) derivatives. Many transposition events among the bz-m(F) selections result in kernels carrying a genetically noncorresponding embryo. These can be interpreted as twin sectors arising at one of the megagametophytic mitoses. The bz locus data fit the earlier (1962) model of I. M. GREENBLATT and R. A. BRINK in which transposition takes place from a replicated donor site to either an unreplicated or replicated receptor site.

摘要

我们研究了 Ac 从易位等位基因 bz-m2(Ac) 中转位的模式。从粗斑点 bz-m2(Ac) 耳中选择了稳定的(bz-s)和细斑点(bz-m(F))的例外。确定基因组中是否存在转位 Ac(trAc),如果存在,则相对于侧翼标记 sh 和 wx 对 trAc 的位置进行映射。Ac 易位到与 bz 相连的位点的一般特征是,受体位点倾向于聚集在 bz 供体位点的任一侧,并且易位是双向的和非极性的。因此,与 bz 相邻的受体位点分布的对称聚类与 I.M.GREENBLATT 于 1984 年报告的 P 位点的不对称聚类不同。尽管 Ac 倾向于优先易位到紧密连锁的位点,但 bz-m2(Ac)中的相当一部分 Ac 易位到非连锁的位点:bz-s 衍生物中为 41%,bz-m(F)衍生物中为 59%。在 bz-m(F)选择中,许多转位事件导致携带遗传上不对应的胚珠的内核。这些可以解释为在一个大配子体有丝分裂中出现的孪生区域。bz 基因座数据符合 I.M.GREENBLATT 和 R.A.BRINK 的早期(1962)模型,即转位从复制的供体位点发生到未复制或复制的受体位点。

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