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本文引用的文献

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Meiotic telomere clustering is inhibited by colchicine but does not require cytoplasmic microtubules.
J Cell Sci. 2002 Oct 1;115(Pt 19):3747-56. doi: 10.1242/jcs.00055.
2
Telomeres act autonomously in maize to organize the meiotic bouquet from a semipolarized chromosome orientation.端粒在玉米中自主发挥作用,从半极化染色体方向组织减数分裂花束。
J Cell Biol. 2002 Apr 15;157(2):231-42. doi: 10.1083/jcb.200110126.
3
Fission yeast mutants affecting telomere clustering and meiosis-specific spindle pole body integrity.影响端粒聚集和减数分裂特异性纺锤体极体完整性的裂殖酵母突变体。
Genetics. 2002 Mar;160(3):861-76. doi: 10.1093/genetics/160.3.861.
4
A bouquet makes ends meet.一束花就能维持收支平衡。 (此译文不太符合常理逻辑,原句可能有误,正常语境下该英文表述可能不太准确表达特定含义,若有正确英文内容可再进行准确翻译)
Nat Rev Mol Cell Biol. 2001 Aug;2(8):621-7. doi: 10.1038/35085086.
5
Nuclear dispositions of subtelomeric and pericentromeric chromosomal domains during meiosis in asynaptic mutants of rye (Secale cereale L.).黑麦(Secale cereale L.)非联会突变体减数分裂过程中染色体亚端粒和着丝粒周围区域的核定位。
J Cell Sci. 2001 May;114(Pt 10):1875-82. doi: 10.1242/jcs.114.10.1875.
6
The polar arrangement of telomeres in interphase and meiosis. Rabl organization and the bouquet.端粒在间期和减数分裂中的极性排列。拉布尔结构和花束。
Plant Physiol. 2001 Feb;125(2):532-8. doi: 10.1104/pp.125.2.532.
7
Mammalian meiotic telomeres: protein composition and redistribution in relation to nuclear pores.哺乳动物减数分裂端粒:与核孔相关的蛋白质组成及重新分布
Mol Biol Cell. 2000 Dec;11(12):4189-203. doi: 10.1091/mbc.11.12.4189.
8
Meiotic telomere protein Ndj1p is required for meiosis-specific telomere distribution, bouquet formation and efficient homologue pairing.减数分裂端粒蛋白Ndj1p是减数分裂特异性端粒分布、花束形成和高效同源配对所必需的。
J Cell Biol. 2000 Oct 2;151(1):95-106. doi: 10.1083/jcb.151.1.95.
9
Evidence for the coincident initiation of homolog pairing and synapsis during the telomere-clustering (bouquet) stage of meiotic prophase.减数分裂前期端粒聚类(花束)阶段同源染色体配对和联会同时起始的证据。
J Cell Sci. 2000 Mar;113 ( Pt 6):1033-42. doi: 10.1242/jcs.113.6.1033.
10
Polyploidy induces centromere association.多倍体诱导着丝粒关联。
J Cell Biol. 2000 Jan 24;148(2):233-8. doi: 10.1083/jcb.148.2.233.

pam1基因是玉米(Zea mays L.)减数分裂花束形成和有效同源联会所必需的。

The pam1 gene is required for meiotic bouquet formation and efficient homologous synapsis in maize (Zea mays L.).

作者信息

Golubovskaya Inna N, Harper Lisa C, Pawlowski Wojciech P, Schichnes Denise, Cande W Zacheus

机构信息

Department of Plant and Microbial Biology, University of California, Berkeley, California 94720-3200, USA.

出版信息

Genetics. 2002 Dec;162(4):1979-93. doi: 10.1093/genetics/162.4.1979.

DOI:10.1093/genetics/162.4.1979
PMID:12524364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1462385/
Abstract

The clustering of telomeres on the nuclear envelope (NE) during meiotic prophase to form the bouquet arrangement of chromosomes may facilitate homologous chromosome synapsis. The pam1 (plural abnormalities of meiosis 1) gene is the first maize gene that appears to be required for telomere clustering, and homologous synapsis is impaired in pam1. Telomere clustering on the NE is arrested or delayed at an intermediate stage in pam1. Telomeres associate with the NE during the leptotene-zygotene transition but cluster slowly if at all as meiosis proceeds. Intermediate stages in telomere clustering including miniclusters are observed in pam1 but not in wild-type meiocytes. The tight bouquet normally seen at zygotene is a rare event. In contrast, the polarization of centromeres vs. telomeres in the nucleus at the leptotene-zygotene transition is the same in mutant and wild-type cells. Defects in homologous chromosome synapsis include incomplete synapsis, nonhomologous synapsis, and unresolved interlocks. However, the number of RAD51 foci on chromosomes in pam1 is similar to that of wild type. We suggest that the defects in homologous synapsis and the retardation of prophase I arise from the irregularity of telomere clustering and propose that pam1 is involved in the control of bouquet formation and downstream meiotic prophase I events.

摘要

减数分裂前期端粒在核膜(NE)上聚集形成染色体花束排列,这可能有助于同源染色体联会。pam1(减数分裂1的多个异常)基因是玉米中第一个似乎是端粒聚集所必需的基因,且pam1中同源联会受损。在pam1中,核膜上的端粒聚集在中间阶段停滞或延迟。端粒在细线期-偶线期转变期间与核膜相关联,但随着减数分裂的进行,端粒聚集缓慢,甚至根本不聚集。在pam1中观察到端粒聚集的中间阶段,包括小聚集体,但在野生型减数分裂细胞中未观察到。通常在偶线期看到的紧密花束是罕见事件。相比之下,在细线期-偶线期转变时,突变细胞和野生型细胞中核内着丝粒与端粒的极化是相同的。同源染色体联会的缺陷包括不完全联会、非同源联会和未解决的互锁。然而,pam1染色体上RAD51焦点的数量与野生型相似。我们认为同源联会缺陷和前期I的延迟源于端粒聚集的不规则性,并提出pam1参与花束形成的控制和下游减数分裂前期I事件。