Reszka A A, Hayashi Y, Horwitz A F
Department of Cell and Structural Biology, University of Illinois, Urbana 61801.
J Cell Biol. 1992 Jun;117(6):1321-30. doi: 10.1083/jcb.117.6.1321.
Wild-type and mutant chicken integrin beta 1 subunit (beta 1c) cDNAs were expressed in NIH 3T3 cells and assayed for localization in focal adhesions of cells plated on fibronectin substrates. Focal adhesion localization in stable transfected cells was assayed by indirect immunofluorescent staining with chicken-specific anti-beta 1c antibodies. Mutant beta 1c integrins containing internal deletions of 13 amino acids adjacent to the membrane, delta 759-771, and 20 centrally located amino acids, delta 771-790, localized in focal adhesions demonstrating that sequences required for direction to focal adhesion structures were not limited to one region of the cytoplasmic domain. Point mutations revealed three clusters of amino acids which contribute to localization in focal adhesions. These three clusters or signals are: cyto-1 (764-774), cyto-2 (785-788), and cyto-3 (797-800). The 11-residue cyto-1 signal is only found on integrin beta subunit sequences, except beta 4. Four residues within this region, D764, F768, F771, and E774, could not be altered without reducing focal adhesion staining intensities, and likely form a signal that occupies one side of an alpha helix. Mutations involving two cyto-1 residues, K770 and F771, also appeared to affect heterodimer affinity and specificity. Cyto-2 (785-788,), NPIY, is an NPXY signal that forms a tight turn motif. Cyto-2 provides a structural conformation, which when perturbed by proline removal or addition, inhibits integrin localization in focal adhesions. Cyto-3 (797-800), NPKY, resembles cyto-2, however, the nonconserved proline residue can be replaced without alteration of the localization phenotype. Cyto-3, therefore, constitutes a unique integrin signal, NXXY. Both serine and tyrosine residues at positions 790 and 788, respectively, which have been implicated in integrin phosphorylation/regulation, were conservatively replaced without detectable effect on focal adhesion localization. However, acidic replacements for these amino acids reduced focal adhesion staining intensities, suggesting that phosphorylation at these sites may negatively regulate integrin function.
野生型和突变型鸡整合素β1亚基(β1c)的cDNA在NIH 3T3细胞中表达,并检测其在铺有纤连蛋白底物的细胞粘着斑中的定位。通过用鸡特异性抗β1c抗体进行间接免疫荧光染色来检测稳定转染细胞中的粘着斑定位。含有膜附近13个氨基酸内部缺失(δ759 - 771)和20个位于中央的氨基酸缺失(δ771 - 790)的突变型β1c整合素定位于粘着斑,这表明引导至粘着斑结构所需的序列不限于细胞质结构域的一个区域。点突变揭示了有助于粘着斑定位的三个氨基酸簇。这三个簇或信号是:细胞内区域1(764 - 774)、细胞内区域2(785 - 788)和细胞内区域3(797 - 800)。11个残基的细胞内区域1信号仅在整合素β亚基序列上发现,但β4除外。该区域内的四个残基,D764、F768、F771和E774,在不降低粘着斑染色强度的情况下不能被改变,并且可能形成占据α螺旋一侧的信号。涉及细胞内区域1的两个残基K770和F771的突变似乎也影响异二聚体的亲和力和特异性。细胞内区域2(785 - 788),NPIY,是一个形成紧密转角基序的NPXY信号。细胞内区域2提供一种结构构象,当通过脯氨酸去除或添加而受到干扰时,会抑制整合素在粘着斑中的定位。细胞内区域3(797 - 800),NPKY,与细胞内区域2相似,然而,非保守的脯氨酸残基可以被替换而不改变定位表型。因此,细胞内区域3构成了一个独特的整合素信号,NXXY。分别在790和788位的丝氨酸和酪氨酸残基,已被证明与整合素磷酸化/调节有关,被保守替换而对粘着斑定位没有可检测到的影响。然而,用酸性氨基酸替换这些氨基酸会降低粘着斑染色强度,这表明这些位点的磷酸化可能对整合素功能产生负调节作用。