Vogan K J, Underhill D A, Gros P
Department of Biochemistry, McGill University, Montreal, Quebec, Canada.
Mol Cell Biol. 1996 Dec;16(12):6677-86. doi: 10.1128/MCB.16.12.6677.
We have identified alternatively spliced isoforms of murine Pax-3 and Pax-7 which differ by the presence or absence of a single glutamine residue in a linker region which separates two distinct DNA-binding subdomains within the paired domain. By reverse transcription-PCR, these isoforms of Pax-3 and Pax-7 (Q+ and Q-) were detected at similar levels through multiple developmental stages in the early mouse embryo. DNA-binding studies using the Q+ and Q- isoforms of Pax-3 revealed that this alternative splicing event had no major effect on the ability of these isoforms to bind to an oligonucleotide specific for the Pax-3 homeodomain (P2) or to a paired domain recognition sequence (e5) that interacts primarily with the N-terminal subdomain of the paired domain. However, DNA-binding studies with sequences (P6CON and CD19-2/A) containing consensus elements for both the N-terminal and C-terminal subdomains revealed that the Q- isoform binds to these sequences with a two- to fivefold-higher affinity; further mutation of the GTCAC core N-terminal subdomain recognition motif of CD19-2/A generated binding sites with a high degree of specificity for the Q- isoform. These differences in DNA binding in vitro were also reflected in the enhanced ability of the Q- isoform to stimulate transcription of a reporter containing multiple copies of CD19-2/A upstream of the thymidine kinase basal promoter. In support of the observations made with these naturally occurring Pax-3 isoforms, introducing a glutamine residue at the analogous position in PAX6 caused a fivefold reduction in binding to P6CON and a complete loss of binding to CD19-2/A and to the C-terminal subdomain-specific probe 5aCON. These studies therefore provide direct evidence for a role for the paired-domain linker region in DNA target site selection, and they identify novel isoforms of Pax-3 and Pax-7 that have the potential to mediate distinct functions in the developing embryo.
我们已经鉴定出小鼠Pax-3和Pax-7的可变剪接异构体,它们在连接区域中存在或不存在单个谷氨酰胺残基而有所不同,该连接区域将配对结构域内两个不同的DNA结合亚结构域分隔开。通过逆转录-聚合酶链反应(RT-PCR),在小鼠早期胚胎的多个发育阶段,以相似水平检测到Pax-3和Pax-7的这些异构体(Q+和Q-)。使用Pax-3的Q+和Q-异构体进行的DNA结合研究表明,这种可变剪接事件对这些异构体与Pax-3同源结构域特异性寡核苷酸(P2)或与主要与配对结构域的N末端亚结构域相互作用的配对结构域识别序列(e5)结合的能力没有重大影响。然而,对含有N末端和C末端亚结构域共有元件的序列(P6CON和CD19-2/A)进行的DNA结合研究表明,Q-异构体与这些序列的结合亲和力高两到五倍;CD19-2/A的GTCAC核心N末端亚结构域识别基序的进一步突变产生了对Q-异构体具有高度特异性的结合位点。体外DNA结合的这些差异也反映在Q-异构体刺激含有胸苷激酶基础启动子上游多个CD19-2/A拷贝的报告基因转录的能力增强上。为了支持对这些天然存在的Pax-3异构体的观察结果,在PAX6的类似位置引入谷氨酰胺残基导致与P6CON的结合减少五倍,并完全丧失与CD19-2/A和C末端亚结构域特异性探针5aCON的结合。因此,这些研究为配对结构域连接区域在DNA靶位点选择中的作用提供了直接证据,并且它们鉴定出Pax-3和Pax-7的新型异构体,这些异构体有可能在发育中的胚胎中介导不同的功能。