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From clonal diversity to transposon derived long non-coding RNA in trematode Himasthla elongata parthenogenetic generations

机译:从克隆多样性到转座子衍生出长期非编码RNA在雷达特霍斯节疟原虫均来世代

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We investigated clonal diversity of parthenogenetic larvae, cercaria, with a simplified AFLP (SAFLP, Amplified fragment length polymorphism) method and explored the nature of diverse zones from electrophoretic patterns. LINE retroelements prevail in fragments analized. One of them was aligned to the spacer region in ORF2 of the CR1-like (LINE class) transposon and named CR1-renegade (CR1-rng). CR1-renegade exists in two types of transcripts: the long ones, containing reverse transcriptase and other domains, and the short ones, containing CR1-rng solely. Probes of CR1 reverse transcriptase (CR1-RT) and CR1-rng yielded strikingly different pictures in FISH physical mapping despite being fragments of CR1 transposons. The CR1-RT probe demonstrated dispersed signal distribution throughout the nuclei and all chromosomes while CR1-rng localized preferentially to the heterochromatic regions. We suppose that CR1-rng transcripts are related to lncRNA regulatory network.
机译:我们调查了床癌幼虫,植物病患者的克隆多样性,具有简化的AFLP(SAFLP,扩增的碎片长度多态性)方法,并探讨了电泳模式的不同区域的性质。在分析的碎片中占上风。其中一个与Cr1样(线类)转座子的ORF2中的间隔区对齐,并命名CR1-REREGADE(CR1-RNG)。 CR1-RENEGADE存在于两种类型的转录物中:长的,含有逆转录酶和其他域,以及仅包含CR1-RNG的短的转录酶和其他域。 Cr1逆转录酶(CR1-RT)和CR1-RNG的探针在鱼物理映射中产生惊人的不同图片,尽管是CR1转座子的碎片。 CR1-RT探针在整个核和所有染色体中证明了分散的信号分布,而优选地定位在异色区。我们假设CR1-RNG成绩单与LNCRNA监管网络有关。

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