Watson Helen R, Butler John, Schuppe Hans-Jürgen, Lee Anthony G, East J Malcolm
Faculty of Life Sciences, University of Manchester, Manchester, UK.
Mol Membr Biol. 2011 May;28(4):216-26. doi: 10.3109/09687688.2011.572566. Epub 2011 Apr 4.
A number of studies using chimeric constructs made by fusing endoplasmic/sarcoplasmic reticulum calcium pump (SERCA) sequences with those of the plasma membrane located calcium pump (PMCA) have suggested that the retention/retrieval signal responsible for maintaining SERCA in the endoplasmic reticulum (ER) is located within the N-terminus of these pumps. Because of the difficulties in identifying the presence of constructs at the plasma membrane we have used a trans-Golgi network (TGN) marker to evaluate whether chimeric proteins are retained by the ER or have lost their retention/retrieval sequences and are able to enter the wider endomembrane system and reach the TGN. In this study, attempts to locate this retention/retrieval sequence demonstrate that the retention sequences are located not in the N-terminus, as previously suggested, but in the largely transmembranous C-terminal domain of SERCA. Further attempts to identify the precise retention/retrieval motif using SERCA1/PMCA3 chimeras were unsuccessful. This may be due to the fact that introducing SERCA1 sequences into the C-terminal PMCA3 sequence and vice versa disrupts the organization of the closely packed transmembrane helices leading to retention of such constructs by the quality control mechanisms of the ER. An alternative explanation is that SERCAs have targeting motifs that are non-linear, being made up of several segments of sequence to form a patch that interacts with the retrieval machinery.
多项研究通过将内质网/肌浆网钙泵(SERCA)序列与质膜钙泵(PMCA)序列融合构建嵌合体,结果表明,负责将SERCA维持在内质网(ER)中的保留/回收信号位于这些泵的N端。由于难以确定质膜上嵌合体的存在情况,我们使用了反式高尔基体网络(TGN)标记来评估嵌合蛋白是被内质网保留,还是失去了其保留/回收序列,从而能够进入更广泛的内膜系统并到达TGN。在本研究中,定位该保留/回收序列的尝试表明,保留序列并非如先前所述位于N端,而是位于SERCA主要为跨膜结构的C端结构域。使用SERCA1/PMCA3嵌合体进一步确定精确保留/回收基序的尝试未成功。这可能是由于将SERCA1序列引入C端PMCA3序列,反之亦然,会破坏紧密堆积的跨膜螺旋的组织,导致这些构建体被内质网的质量控制机制保留。另一种解释是,SERCA具有非线性的靶向基序,由几个序列片段组成一个补丁,与回收机制相互作用。