Šťáhlavský František, Forman Martin, Just Pavel, Denič Filip, Haddad Charles R, Opatova Vera
Department of Zoology, Charles University, Faculty of Science, Viničná 7, CZ-12844 Praha, Czech Republic.
Department of Genetics and Microbiology, Charles University, Faculty of Science, Viničná 5, CZ-12844 Praha, Czech Republic.
Comp Cytogenet. 2020 Mar 4;14(1):107-138. doi: 10.3897/CompCytogen.v14i1.48667. eCollection 2020.
Spiders represent one of the most studied arachnid orders. They are particularly intriguing from a cytogenetic point of view, due to their complex and dynamic sex chromosome determination systems. Despite intensive research on this group, cytogenetic data from African spiders are still mostly lacking. In this study, we describe the karyotypes of 38 species of spiders belonging to 16 entelegyne families from South Africa and Namibia. In the majority of analysed families, the observed chromosome numbers and morphology (mainly acrocentric) did not deviate from the family-level cytogenetic characteristics based on material from other continents: Tetragnathidae (2n♂ = 24), Ctenidae and Oxyopidae (2n♂ = 28), Sparassidae (2n♂ = 42), Gnaphosidae, Trachelidae and Trochanteriidae (2n♂ = 22), and Salticidae (2n♂ = 28). On the other hand, we identified interspecific variability within Hersiliidae (2n♂ = 33 and 35), Oecobiidae (2n♂ = 19 and 25), Selenopidae (2n♂ = 26 and 29) and Theridiidae (2n♂ = 21 and 22). We examined the karyotypes of Ammoxenidae and Gallieniellidae for the first time. Their diploid counts (2n♂ = 22) correspond to the superfamily Gnaphosoidea and support their placement in this lineage. On the other hand, the karyotypes of Prodidominae (2n♂ = 28 and 29) contrast with all other Gnaphosoidea. Similarly, the unusually high diploid number in sp. (2n♂ = 28) within the otherwise cytogenetically uniform family Thomisidae (mainly 2n♂ = 21-24) supports molecular data suggesting a basal position of the genus in the family. The implementation of FISH methods for visualisation of rDNA clusters facilitated the detection of complex dynamics of numbers of these loci. We identified up to five loci of the 18S rDNA clusters in our samples. Three different sex chromosome systems (X0, XX0 and XXX0) were also detected among the studied taxa.
蜘蛛是研究最为深入的蛛形纲目之一。从细胞遗传学角度来看,它们尤其引人关注,因为其具有复杂且动态的性染色体决定系统。尽管对该类群进行了大量研究,但非洲蜘蛛的细胞遗传学数据仍然十分匮乏。在本研究中,我们描述了来自南非和纳米比亚的16个栉足蛛科家族的38种蜘蛛的核型。在大多数分析的家族中,观察到的染色体数目和形态(主要为近端着丝粒染色体)与基于其他大陆材料得出的科级细胞遗传学特征并无偏差:肖蛸科(2n♂ = 24)、栉足蛛科和猫蛛科(2n♂ = 28)、蟹蛛科(2n♂ = 42)、平腹蛛科、管蛛科和奇蛛科(2n♂ = 22)以及跳蛛科(2n♂ = 28)。另一方面,我们在希蛛科(2n♂ = 33和35)、巢蛛科(2n♂ = 19和25)、妖面蛛科(2n♂ = 26和29)和球蛛科(2n♂ = 21和22)中发现了种间变异性。我们首次研究了暗蛛科和加利蛛科的核型。它们的二倍体数目(2n♂ = 22)与平腹蛛总科相符,并支持它们在该谱系中的分类地位。另一方面,原遁蛛亚科(2n♂ = 28和29)的核型与所有其他平腹蛛总科不同。同样,在细胞遗传学上原本较为一致的蟹蛛科(主要为2n♂ = 21 - 24)中,某种蜘蛛(2n♂ = 28)异常高的二倍体数目支持了分子数据所表明的该属在科内的基部位置。荧光原位杂交(FISH)方法用于可视化核糖体DNA(rDNA)簇,有助于检测这些位点数量的复杂动态变化。我们在样本中鉴定出多达5个18S rDNA簇位点。在所研究的分类单元中还检测到三种不同的性染色体系统(X0、XX0和XXX0)。