Donev Rossen, Horton Roger, Beck Stephan, Doneva Teodora, Vatcheva Radost, Bowen W Richard, Sheer Denise
Human Cytogenetics Laboratory, Cancer Research, UK London Research Institute, Lincoln's Inn Fields Laboratories, 44 Lincoln's Inn Fields, London WC2A 3PX, United Kingdom.
J Biol Chem. 2003 Feb 14;278(7):5214-26. doi: 10.1074/jbc.M206621200. Epub 2002 Nov 14.
Sequences containing the matrix recognition signature were identified adjacent to the LMP/TAP gene cluster in the human and mouse major histocompatibility complex class II region. These sequences were shown to function as nuclear matrix attachment regions (MARs). Three of the five human MARs and the single mouse MAR recruit heterogeneous nuclear ribonucleoprotein A1 (hnRNP-A1) in vivo during transcriptional up-regulation of the major histocompatibility complex class II genes. The timing of this recruitment correlates with a rise in mature TAP1 mRNA. Two of the human MARs bind hnRNP-A1 in vitro directly within a 35-bp sequence that shows over 90% similarity to certain Alu repeat sequences. This study shows that MARs recruit and bind hnRNP-A1 upon transcriptional up-regulation.
在人类和小鼠主要组织相容性复合体II类区域中,紧邻LMP/TAP基因簇鉴定出了含有基质识别特征的序列。这些序列被证明具有核基质附着区域(MARs)的功能。在主要组织相容性复合体II类基因转录上调期间,五个人类MARs中的三个以及单个小鼠MARs在体内招募异质性核糖核蛋白A1(hnRNP-A1)。这种招募的时间与成熟TAP1 mRNA的增加相关。两个人类MARs在体外能在一个35碱基对序列内直接结合hnRNP-A1,该序列与某些Alu重复序列具有超过90%的相似性。这项研究表明,MARs在转录上调时招募并结合hnRNP-A1。