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Pachytene analysis in a 17;21 reciprocal translocation carrier: role of the acrocentric chromosomes in male sterility.

作者信息

Luciani J M, Guichaoua M R, Delafontaine D, North M O, Gabriel-Robez O, Rumpler Y

机构信息

Départment d'Embryologie et de Cytogénétique, Faculté de Médecine, Marseille, France.

出版信息

Hum Genet. 1987 Nov;77(3):246-50. doi: 10.1007/BF00284478.

DOI:10.1007/BF00284478
PMID:3679209
Abstract

Pachytene analysis was undertaken in an infertile male, heterozygous for a 17;21 reciprocal translocation. The quadrivalent was identified by its configuration and chromomere pattern. A non-random association was found between the quadrivalent and the sex vesicle in 77% of the pachytene nuclei analysed. In 13.1% of the cells the contact with the sex vesicle was established by the terminal chromomere of the two chromosomes 21; in 63.9% of the cells, the entire region of the breakpoints was completely hidden by the sex vesicle. In some nuclei asynapsis was found in the region of the breakpoints. The nature of the contact between the quadrivalent and the sex vesicle is discussed in this paper. It is proposed that the acrocentric chromosome favours the contact between the quadrivalent and the sex vesicle, and increases the risk of sterility in male carriers of Robertsonian translocations and of reciprocal translocations involving one acrocentric chromosome.

摘要

相似文献

1
Pachytene analysis in a 17;21 reciprocal translocation carrier: role of the acrocentric chromosomes in male sterility.
Hum Genet. 1987 Nov;77(3):246-50. doi: 10.1007/BF00284478.
2
[Pachytene stage of meiosis in an infertile man carrying a reciprocal translocation between two acrocentric chromosomes].
Ann Genet. 1994;37(1):26-9.
3
Meiotic association between the XY chromosomes and the autosomal quadrivalent of a reciprocal translocation in two infertile men, 46,XY,t(19;22) and 46,XY,t(17;21).两名46,XY,t(19;22)和46,XY,t(17;21)的不育男性中XY染色体与相互易位的常染色体四价体之间的减数分裂关联
Cytogenet Cell Genet. 1986;43(3-4):154-60. doi: 10.1159/000132314.
4
[Analysis of synaptonemal complex from a carrier with 46,XY,t(11;18) balanced translocation].[对一名46,XY,t(11;18)平衡易位携带者的联会复合体分析]
Yi Chuan Xue Bao. 2004 Feb;31(2):125-31.
5
XY-quadrivalent association and sterility in a man carrier of a reciprocal autosomal translocation involving the whole arm of an acrocentric chromosome t(2;15)(q21.3;cen).
Andrologia. 1995 May-Jun;27(3):171-4. doi: 10.1111/j.1439-0272.1995.tb01090.x.
6
Pachytene analysis of a man with a 13q;14q translocation and infertility. Behavior of the trivalent and nonrandom association with the sex vesicle.一名患有13号染色体与14号染色体易位及不育症男性的粗线期分析。三价体的行为及与性泡的非随机关联。
Cytogenet Cell Genet. 1984;38(1):14-22. doi: 10.1159/000132023.
7
Three dimensional reconstruction of human pachytene spermatocyte nuclei of a 17;21 reciprocal translocation carrier: study of XY-autosome relationships.一名17;21相互易位携带者的人类粗线期精母细胞核的三维重建:XY-常染色体关系研究
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Analysis of synaptonemal complexes in a heterozygous human male carrier of a reciprocal translocation involving an acrocentric chromosome: heterosynapsis without previous homosynapsis.对一名涉及近端着丝粒染色体的相互易位杂合子男性携带者的联会复合体进行分析:未出现前期同源联会的异源联会。
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9
Chromosomal anomalies and disturbance of transcriptional activity at the pachytene stage of meiosis: relationship to male sterility.减数分裂粗线期的染色体异常与转录活性紊乱:与雄性不育的关系。
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Pachytene chromosomes in trisomy 19 male mice with Robertsonian translocations.患有罗伯逊易位的19三体雄性小鼠的粗线期染色体。
Chromosome Res. 1998 Jun;6(4):285-94. doi: 10.1023/a:1009218807304.

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Numerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization.通过荧光原位杂交检测的生育能力正常和不育男性精子中的染色体数目异常

本文引用的文献

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A pericentric inversion in the mouse.
Cytogenet Cell Genet. 1981;30(2):70-6. doi: 10.1159/000131593.
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Male infertility in a case of (Y; 6) balanced reciprocal translocation. Mitotic and meiotic study.一例(Y;6)平衡易位导致的男性不育。有丝分裂和减数分裂研究。
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Complete pachytene chromomere karyotypes of human spermatocyte bivalents.人类精母细胞二价体的完整粗线期染色粒核型
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Chromosomally derived sterile mice have a 'fertile' active XY chromatin conformation but no XY body.染色体衍生的不育小鼠具有“可育”的活跃XY染色质构象,但没有XY小体。
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Infertility in human males with autosomal translocations: meiotic study of a 14;22 Robertsonian translocation.常染色体易位男性的不育症:14;22罗伯逊易位的减数分裂研究
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Three dimensional reconstruction of human pachytene spermatocyte nuclei of a 17;21 reciprocal translocation carrier: study of XY-autosome relationships.一名17;21相互易位携带者的人类粗线期精母细胞核的三维重建:XY-常染色体关系研究
Hum Genet. 1991 Oct;87(6):709-15. doi: 10.1007/BF00201730.
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The association of the nucleolus and the short arm of acrocentric chromosomes with the XY pair in human spermatocytes: its possible role in facilitating sex-chromosome acrocentric translocations.人类精母细胞中核仁、近端着丝粒染色体短臂与XY染色体对的关联:其在促进性染色体近端着丝粒易位中可能发挥的作用。
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Hum Genet. 1983;63(2):132-8. doi: 10.1007/BF00291532.
6
Pachytene analysis of a man with a 13q;14q translocation and infertility. Behavior of the trivalent and nonrandom association with the sex vesicle.一名患有13号染色体与14号染色体易位及不育症男性的粗线期分析。三价体的行为及与性泡的非随机关联。
Cytogenet Cell Genet. 1984;38(1):14-22. doi: 10.1159/000132023.
7
XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocytes of the mouse (Mus musculus).XY 配对与小鼠(小家鼠)粗线期精母细胞中常染色体雄性不育易位的联会复合体相关。
Chromosoma. 1981;82(1):41-53. doi: 10.1007/BF00285748.
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The three-dimensional reconstruction of the XY chromosomal pair in human spermatocytes.人类精母细胞中XY染色体对的三维重建。
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[Meiotic chromosomes of humans. II. The nucleolus. The chiasmata. 3. Male sterility].[人类减数分裂染色体。II. 核仁。交叉。3. 雄性不育]
Ann Genet. 1970 Sep;13(3):169-82.
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Sex-chromosome pairing and male fertility.性染色体配对与男性生育能力。
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