首页> 外文期刊>Cytogenetic and genome research >Mapping the distribution of the telomeric sequence (T(2)AG(3))(n) in rock wallabies, Petrogale (Marsupialia: Macropodidae), by fluorescence in situ hybridization. ii. the lateralis complex.
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Mapping the distribution of the telomeric sequence (T(2)AG(3))(n) in rock wallabies, Petrogale (Marsupialia: Macropodidae), by fluorescence in situ hybridization. ii. the lateralis complex.

机译:映射端粒序列(T(2)AG(3))(n)在岩石小袋鼠,Petrogale(Marsupialia:Macropodidae),通过荧光原位杂交的分布。 ii。横向复杂。

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摘要

The distribution of the conserved vertebrate telomeric sequence (T(2)AG(3))(n) was examined by fluorescence in situ hybridization in the six Petrogale (rock wallabies) taxa of the lateralis complex. As expected, the (T(2)AG(3))(n) sequence was located at the termini of all chromosomes in all taxa. However, the sequence was also present at several nontelomeric (viz., interstitial and centromeric) sites. The signals identified were associated with either ancient rearrangements involved with the formation of the 2n = 22 plesiomorphic macropodine karyotype or more recent rearrangements associated with karyotypes derived from the 2n = 22 karyotype. Interstitial (T(2)AG(3))(n) signals identified on chromosomes 3 and 4 in all six species of the lateralis complex and a large centromeric signal identified on chromosome 7 in the five subspecies/races of P. lateralis appear to be related to the more ancient rearrangements. Subsequent chromosome evolution has seen these signals retained, lost, or amplified in different Petrogale lineages. Within the lateralis complex, in two submetacentric chromosome derived by recent centric fusions, the telomeric sequence was identified at or near the centromere, indicating its retention during the fusion process. In the two taxa where chromosome 3 was rearranged via a recent centromeric transposition to become an acrocentric chromosome, the telomeric signal was located interstitially.
机译:守恒的脊椎动物端粒序列(T(2)AG(3))(n)的分布通过荧光原位杂交在侧枝复合体的六个Petrogale(岩袋鼠)类群中进行了检查。如预期的那样,(T(2)AG(3))(n)序列位于所有分类单元中所有染色体的末端。但是,该序列也存在于几个非端粒(即间质和着丝粒)位点。鉴定出的信号与涉及2n = 22多态性大脚鱼核型形成的古老重排有关,或者与源自2n = 22核型的核型相关的更近期重排有关。在侧枝复合体的所有六个物种的第3和4号染色体上鉴定到的间质性(T(2)AG(3))(n)信号似乎在侧枝假单胞菌的五个亚种/种族中在染色体7上鉴定出的大着丝粒信号似乎与更古老的重新安排有关。随后的染色体进化已经看到这些信号在不同的Petrogale谱系中保留,丢失或放大。在侧向复合体中,在由最近的中心融合产生的两个亚超中心染色体中,端粒序列在着丝粒处或附近被鉴定,表明其在融合过程中得以保留。在两个分类单元中,染色体3通过最近的着丝粒转座重新排列,成为近端染色体,端粒信号位于间隙中。

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