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胸腺细胞核环状DNA中的T细胞受体β基因序列:V-D-J连接中分子内DNA缺失的直接证据。

T cell receptor beta gene sequences in the circular DNA of thymocyte nuclei: direct evidence for intramolecular DNA deletion in V-D-J joining.

作者信息

Okazaki K, Davis D D, Sakano H

出版信息

Cell. 1987 May 22;49(4):477-85. doi: 10.1016/0092-8674(87)90450-8.

Abstract

We have identified circular DNA containing T cell receptor (TCR) beta gene sequences in mouse thymocytes, thereby providing direct evidence for the intramolecular DNA deletion model of V-D-J joining in TCR beta genes. Two types of excision products of V-D-J joining have been identified. Type I, a circular reciprocal recombinant of normal V-D or D-J joining, contains a 7mer-7mer head-to-head structure expected from an excised product of normal V-D or D-J joining. Type II contains a D beta 2-J beta 1 structure on the circular DNA; the recombination event producing this molecule occurs between an upstream J and a downstream D segment, probably leaving the reciprocal 7mer-7mer structure on the chromosome. Some type I molecules seem to represent excision products of secondary joining after formation of the first D-J or V-D-J structure. The recombination mechanism that generates the circular DNA is discussed.

摘要

我们已经在小鼠胸腺细胞中鉴定出含有T细胞受体(TCR)β基因序列的环状DNA,从而为TCRβ基因中V-D-J连接的分子内DNA缺失模型提供了直接证据。已鉴定出V-D-J连接的两种类型的切除产物。I型是正常V-D或D-J连接的环状相互重组体,包含正常V-D或D-J连接的切除产物预期的7聚体-7聚体头对头结构。II型在环状DNA上含有Dβ2-Jβ1结构;产生该分子的重组事件发生在上游J和下游D片段之间,可能在染色体上留下相互的7聚体-7聚体结构。一些I型分子似乎代表在第一个D-J或V-D-J结构形成后二次连接的切除产物。文中讨论了产生环状DNA的重组机制。

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