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Sequence heterogeneity within the human alphoid repetitive DNA family.

机译:人类Alphaid重复DNA家族中的序列异质性。

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摘要

We have cloned and determined the base-sequence and genome organization of two human chromosome-specific alphoid DNA fragments, designated L1.26, mapping principally to chromosomes 13 and 21, and L1.84, mapping to chromosome 18. Their copy number is estimated to be approximately 2,000 per haploid genome. L1.84 has a double-dimer organization, whereas L1.26 has a much less defined higher order tandem organization. Further, we present evidence that the restriction-site spacing within the alphoid DNA family is chromosome specific. From sequence analysis, clones L1.26 and L1.84 are found to consist of 5 and 4 tandemly duplicated 170 bp monomers. Cross-homology between the various monomers is 65-85%. The analysis suggests that the evolution of tandem-arrays does not take place via a defined 340 bp unit, as was inferred by others, but via circularly permutated monomers or multimers of the 170 bp unit.
机译:我们已经克隆并确定了两个人类染色体特有的脂质类DNA片段的碱基序列和基因组结构,命名为L1.26,主要定位于13和21号染色体,L1.84,定位于18号染色体。估计了它们的拷贝数每个单倍体基因组大约2,000。 L1.84具有双二聚体组织,而L1.26具有定义不多的高阶串联组织。此外,我们目前的证据表明,在Alphaid DNA家族内的限制性位点间隔是染色体特异性的。通过序列分析,发现克隆L1.26和L1.84由5个和4个串联重复的170bp单体组成。各种单体之间的交叉同源性是65-85%。分析表明,串联阵列的进化不是像其他人所推断的那样,通过一个确定的340 bp单元发生的,而是通过环状排列的单体或170 bp单元的多聚体发生的。

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