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小鼠蛋白酶体亚基DELTA(Lmp19)编码基因的表征与定位

Characterization and mapping of the gene encoding mouse proteasome subunit DELTA (Lmp19).

作者信息

Woodward E C, Monaco J J

机构信息

Department of Microbiology and Immunology, Virginia Commonwealth University, Richmond 23298, USA.

出版信息

Immunogenetics. 1995;42(1):28-34. doi: 10.1007/BF00164984.

Abstract

The proteasome subunit DELTA is unusually closely related to the major histocompatibility complex (MHC)-linked proteasome subunit, LMP2. The sequence of a mouse cDNA for DELTA confirms that this 22,100 M(r) proteasome subunit is highly conserved across species. Sequence analysis of the mouse gene encoding DELTA, designated Lmp19, indicates that it consists of six exons and five introns, similar to the Lmp2 gene. The 5' upstream region lacks a TATA regulatory sequence, which is also absent from proteasome genes isolated from Drosophila. BXD recombinant inbred (RI) mice were used to map the potential chromosomal location of Lmp19, and revealed that the DELTA subunit has related sequences present on two different mouse chromosomes, chromosomes 1 and 11. Typing of 89 progeny from a C57BL/6J X Mus spretus DNA backcross panel (BSS) confirmed the chromosome 1 assignment. Southern hybridization with a polymerase chain reaction-generated Lmp19 intron 2-specific probe indicates that the Lmp19 genomic clone corresponds to the sequence on chromosome 11, and further suggests that the chromosome 1 copy represents a processed pseudogene (Lmp19-ps1).

摘要

蛋白酶体亚基DELTA与主要组织相容性复合体(MHC)相关蛋白酶体亚基LMP2异常密切相关。小鼠DELTA cDNA序列证实,这个分子量为22,100的蛋白酶体亚基在物种间高度保守。对编码DELTA的小鼠基因(命名为Lmp19)的序列分析表明,它由六个外显子和五个内含子组成,与Lmp2基因相似。其5'上游区域缺乏TATA调控序列,从果蝇中分离出的蛋白酶体基因也没有该序列。利用BXD重组近交(RI)小鼠对Lmp19的潜在染色体定位进行了图谱绘制,结果显示DELTA亚基在小鼠的两条不同染色体(1号和11号染色体)上存在相关序列。对C57BL/6J×小家鼠DNA回交群体(BSS)的89个后代进行分型,证实了1号染色体的定位。用聚合酶链反应产生的Lmp19内含子2特异性探针进行Southern杂交,表明Lmp19基因组克隆对应于11号染色体上的序列,进一步表明1号染色体上的拷贝代表一个加工后的假基因(Lmp19-ps1)。

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