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在A20/2J B细胞淋巴瘤中H-2Eb与一个IAP逆转录转座子的相互作用。

Interaction of H-2Eb with an IAP retrotransposon in the A20/2J B cell lymphoma.

作者信息

Malstrom C E, Kotsenas A L, Jones B

机构信息

Department of Molecular and Cell Biology, Pennsylvania State University, University Park 16802.

出版信息

Immunogenetics. 1992;36(4):238-47. doi: 10.1007/BF00215054.

Abstract

In the A20/2J BALB/c B cell lymphoma, Southern analysis revealed an insertion of approximately 6 kilobases of DNA into the first intron of one Ebd-allele. Two observations suggest that the rearrangement did not occur recently in the A20/2J subline. Firstly, normal and altered Ebd-alleles are present in equal numbers, and secondly, the LB 27.4 and LS 102.9 somatic cell hybrids formed at an earlier date both possess the rearrangement. Sequences of two cDNA clones, lambda Eb-7 and lambda Eb-125, selected from an A20/2J cDNA library prepared from poly [A+] RNA indicate that the rearranged Ebd-allele directs the synthesis of atypical Eb transcripts. The clones contain Eb sequence linked to a portion of retroviral-like intracisternal A-particle (IAP) genomic sequence, and they appear to be copies of mRNA produced by splicing between a 5' donor site in the retroviral transcript and the 3' acceptor site of the Eb gene's first intron. The longer lambda Eb-125 insert corresponds to RNA that initiated in the 5'-untranslated region of the Eb gene. The 3'-end of the first Eb exon joins to long terminal repeat sequence, and retroviral sequence extends up to the splice junction with the second Eb exon; 3' of the junction, the lambda Eb-125 sequence corresponds to that of a correctly spliced Eb transcript. It seems feasible that the cDNA clones represent hybrid RNA synthesized by read-through transcription of the Eb coding region and an IAP element inserted into the first intron of the rearranged Ebd-allele.

摘要

在A20/2J BALB/c B细胞淋巴瘤中,Southern印迹分析显示,在一个Ebd等位基因的第一个内含子中插入了约6千碱基的DNA。两项观察结果表明,这种重排在A20/2J亚系中并非近期发生。首先,正常和改变的Ebd等位基因数量相等;其次,早期形成的LB 27.4和LS 102.9体细胞杂种都具有这种重排。从由聚腺苷酸[poly(A+)]RNA制备的A20/2J cDNA文库中选出的两个cDNA克隆(λEb-7和λEb-125)的序列表明,重排的Ebd等位基因指导合成非典型的Eb转录本。这些克隆包含与部分逆转录病毒样胞内A颗粒(IAP)基因组序列相连的Eb序列,它们似乎是通过逆转录病毒转录本中的5'供体位点与Eb基因第一个内含子的3'受体位点之间的剪接产生的mRNA的拷贝。较长的λEb-125插入片段对应于在Eb基因5'非翻译区起始的RNA。第一个Eb外显子的3'端与长末端重复序列相连,逆转录病毒序列一直延伸到与第二个Eb外显子的剪接连接处;在连接处的3'端,λEb-125序列与正确剪接的Eb转录本的序列相对应。这些cDNA克隆代表由Eb编码区的通读转录和插入到重排的Ebd等位基因第一个内含子中的IAP元件合成的杂合RNA,这似乎是可行的。

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