首页> 美国卫生研究院文献>Nucleic Acids Research >Presence of a polyadenylated RNA fragment encoding the membrane domain for immunoglobulin alpha chain indicates that mRNAs for both secreted and membrane-bound alpha chains can be produced from the same RNA transcript.
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Presence of a polyadenylated RNA fragment encoding the membrane domain for immunoglobulin alpha chain indicates that mRNAs for both secreted and membrane-bound alpha chains can be produced from the same RNA transcript.

机译:编码免疫球蛋白α链膜结构域的聚腺苷酸化RNA片段的存在表明分泌的和膜结合的α链的mRNA均可从同一RNA转录物中产生。

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摘要

RNA blotting was employed to examine polyadenylated immunoglobulin alpha chain RNAs in a B lymphoma synthesizing membrane-bound and secretory IgA and in a hybridoma which synthesizes predominantly secretory IgA. Both cell lines were derived from the I.29 lymphoma and expressed the identical heavy chain variable region gene. In addition to the predicted mRNA precursors, four novel species of polyadenylated alpha RNAs were detected. The presence of a RNA species which was too large to have the same 3' end as the largest mRNA for membrane-bound alpha chain (alpha m) implied that transcription continued past the alpha m poly(A) site, and that such transcripts could be polyadenylated. Alternatively, transcription of this alpha RNA was initiated 5' to the normal cap site. Two species of RNA were detected which encoded the alpha m domain and the intervening sequence between the alpha constant (C alpha) and alpha m domain but not the C alpha domain. These RNA molecules were of sizes appropriate for their derivation by endonucleolytic cleavage of a precursor for alpha m mRNA at the poly(A) site of the mRNA for secreted alpha chains (alpha s). The presence of these three alpha RNA species suggested that alternative and successive cleavage/polyadenylation events could occur on a single transcript to produce either alpha m or alpha s mRNAs. An additional novel species of RNA was detected which indicated that the order of removal of the large IVSs did not always proceed in the 5' to 3' direction.
机译:RNA印迹法用于在合成膜结合和分泌型IgA的B淋巴瘤和主要合成分泌型IgA的杂交瘤中检查多腺苷酸化免疫球蛋白α链RNA。两种细胞系均来自I.29淋巴瘤,并表达相同的重链可变区基因。除了预测的mRNA前体,还检测到四种新型的聚腺苷酸化αRNA。 RNA物种的存在太大,无法与膜结合的α链(alpha m)的最大mRNA的3'端具有相同的3'端,这意味着转录持续超过alpha m poly(A)位点,并且此类转录本可以被聚腺苷酸化。或者,此αRNA的转录起始于正常帽的5'端。检测到两种RNA,它们编码αm结构域以及α常数(C alpha)和αm结构域之间的插入序列,但不编码C alpha结构域。这些RNA分子的大小适合于通过在分泌的α链(alpha s)的mRNA的poly(A)位点对αm mRNA的前体进行内切核酸酶裂解而得到的大小。这三个αRNA种类的存在表明,在单个转录本上可能会发生交替和连续的切割/聚腺苷酸化事件,从而产生αm或αs mRNA。检测到另一种新颖的RNA,表明大型IVS的去除顺序并不总是沿5'至3'方向进行。

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