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A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination.

作者信息

Blouin J L, Christie D H, Gos A, Lynn A, Morris M A, Ledbetter D H, Chakravarti A, Antonarakis S E

机构信息

Division of Medical Genetics, Cantonal Hospital of Geneva, Switzerland.

出版信息

Am J Hum Genet. 1995 Aug;57(2):388-94.

PMID:7668265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1801529/
Abstract

We have used a half-YAC containing the human chromosome 21 long-arm telomere to clone, map, and characterize a new dinucleotide repeat polymorphism (D21S1575) close to 21qter. This marker is < 120 kb from the telomeric (TTAGGG)n sequences and is the most distal highly polymorphic marker on chromosome 21q. This marker has a heterozygosity of 71% because of a variable (TA)n repeat embedded within a long interspersed element (LINE) element. Genotyping of the CEPH families and linkage analysis provided a more accurate determination of the full length of the chromosome 21 genetic map. A highly significant difference was detected between male and female recombination rates in the telomeric region: in the most telomeric 2.3 Mb of chromosome 21q, recombination was only observed in male meioses.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e6/1801529/39f3e5d2581a/ajhg00034-0198-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e6/1801529/11d00e1fc6a0/ajhg00034-0196-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e6/1801529/2c3cb40172b2/ajhg00034-0197-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e6/1801529/39f3e5d2581a/ajhg00034-0198-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e6/1801529/11d00e1fc6a0/ajhg00034-0196-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e6/1801529/2c3cb40172b2/ajhg00034-0197-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e6/1801529/39f3e5d2581a/ajhg00034-0198-a.jpg

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引用本文的文献

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本文引用的文献

1
Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age.体细胞中的有丝分裂错误在约4.5%的病例中导致21三体,且与母亲高龄无关。
Nat Genet. 1993 Feb;3(2):146-50. doi: 10.1038/ng0293-146.
2
Molecular characterization of a pericentric inversion in mouse chromosome 8 implicates telomeres as promoters of meiotic recombination.小鼠8号染色体臂间倒位的分子特征表明端粒是减数分裂重组的启动子。
Chromosoma. 1993 Jan;102(2):112-20. doi: 10.1007/BF00356028.
3
A "hot spot" of recombination coincides with an interstitial telomeric sequence in the Armenian hamster.
人类家系中与年龄相关的重组率。
PLoS Genet. 2011 Sep;7(9):e1002251. doi: 10.1371/journal.pgen.1002251. Epub 2011 Sep 1.
4
Subtelomeric rearrangements in idiopathic mental retardation.特发性智力障碍中的亚端粒重排
Indian J Pediatr. 2005 Aug;72(8):679-85. doi: 10.1007/BF02724077.
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Characterization of physical gap sizes at human telomeres.人类端粒处物理间隙大小的表征
Genome Res. 1999 Sep;9(9):888-94. doi: 10.1101/gr.9.9.888.
6
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type-A/B; No phenotype prediction from the position of GLI3 mutations.GLI3形态病变的表型谱包括常染色体显性遗传的IV型轴前多指畸形和A/B型轴后多指畸形;无法根据GLI3突变的位置预测表型。
Am J Hum Genet. 1999 Sep;65(3):645-55. doi: 10.1086/302557.
7
Evidence for effective suppression of recombination in the chromosome 17q21 segment spanning RNU2-BRCA1.在跨越RNU2 - BRCA1的17号染色体q21区段有效抑制重组的证据。
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Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.黑斑息肉综合征:确认与19号染色体p13.3区域连锁,并在19号染色体q13.4区域鉴定出一个潜在的第二基因座。
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