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新的复杂X-Y-常染色体易位及扩增异染色质在鹿角花金龟(桑德斯)(鞘翅目,金龟科,花金龟亚科)中的减数分裂行为

Meiotic behaviour of a new complex X-Y-autosome translocation and amplified heterochromatin in Jumnos ruckeri (Saunders) (Coleoptera, Scarabaeidae, Cetoniinae).

作者信息

Macaisne N, Dutrillaux A M, Dutrillaux B

机构信息

UMR 5202 CNRS/MNHN, Organisation, Structure et Evolution de la Biodiversité, Muséum National d'Histoire Naturelle, CP 39, 16, rue Buffon, Paris, 75005, France.

出版信息

Chromosome Res. 2006;14(8):909-18. doi: 10.1007/s10577-006-1098-6. Epub 2007 Jan 19.

Abstract

Species belonging to the Cetoniinae subfamily studied so far possess 20 chromosomes, including a small X and a punctiform Y: 20,Xyp in the males. In a series of species from the Goliathini tribe under study we found a very unusual karyotype, with 12 autosomes and large sex chromosomes (14,neoXY) in Jumnos ruckieri from Thailand. Applying various techniques including pachytene bivalent spreading, we showed that 40% (mitotic and meiotic prophases) to 60% (metaphases) of the karyotype length was composed of heterochromatin. Both sex chromosomes were NOR carriers. At pachynema they underwent a complete synapsis of their distal regions, indicating their autosomal origin. At contrast, their very uneven central regions remained separated, but associated with nucleolus material. This association persisted until diakinesis, forming a pseudo-chiasma between the neoX and the neoY, which were always in end-to-end association. Compared to free autosomes the autosomal parts of the neo-sex chromosomes had a significant lack of interstitial chiasmata, indicating a possible lack of recombination at their proximal regions. As in the cases of X-autosome translocations in mammals, autosomal and gonosomal parts of the neo-sex chromosomes were insulated by heterochromatin, which may be a necessary condition to avoid deleterious position effects, whatever the mechanisms of gene dosage compensation.

摘要

迄今为止所研究的花金龟亚科物种拥有20条染色体,包括一条小的X染色体和一条点状Y染色体:雄性为20,Xyp。在一系列正在研究的巨花金龟族物种中,我们在泰国的鲁氏巨花金龟中发现了一种非常不寻常的核型,有12条常染色体和大的性染色体(14,neoXY)。应用包括粗线期二价体铺展在内的各种技术,我们发现核型长度的40%(有丝分裂和减数分裂前期)到60%(中期)由异染色质组成。两条性染色体都是核仁组织区(NOR)携带者。在粗线期,它们的远端区域完全联会,表明它们起源于常染色体。相比之下,它们非常不均匀的中央区域仍然分离,但与核仁物质相关。这种关联一直持续到终变期,在neoX和neoY之间形成一个假交叉,它们总是端对端相连。与游离的常染色体相比,新性染色体的常染色体部分明显缺乏中间交叉,表明其近端区域可能缺乏重组。就像哺乳动物中X染色体与常染色体易位的情况一样,新性染色体的常染色体部分和性染色体部分被异染色质隔开,无论基因剂量补偿的机制如何,这可能是避免有害位置效应的必要条件。

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