Iavarone A, Garg P, Lasorella A, Hsu J, Israel M A
Preuss Laboratory, Department of Neurological Surgery, School of Medicine, University of California, San Francisco 94143.
Genes Dev. 1994 Jun 1;8(11):1270-84. doi: 10.1101/gad.8.11.1270.
Cell growth and differentiation are usually antagonistic. Proteins of the basic helix-loop-helix (bHLH) family bind DNA and play important roles in the differentiation of specific cell types. Id proteins heterodimerize with bHLH transcription factors, blocking their activation of lineage-specific gene expression and thereby inhibiting cellular differentiation. To examine the effect of Id-2 on cell proliferation, we overexpressed Id-2 in the human osteosarcoma cell line U2OS. Id-2 expression in U2OS reduced the serum requirement for growth and stimulated cellular proliferation by shortening the doubling time and increasing the percentage of cells in S phase. We demonstrated that Id-2 expression was able to reverse the inhibition of cellular proliferation and the block in cell cycle progression mediated by the product of the retinoblastoma tumor suppressor gene pRB. This effect was not associated with changes in the state of pRb phosphorylation in transfected cells. In vitro, unphosphorylated pRb from cell lysates specifically bound Id-2 but was not able to bind a mutated form of Id-2 lacking the HLH domain that also did not antagonize the growth arrest by pRb. In vitro-synthesized pRb containing mutations within the E1A/large T-binding pocket did not bind Id-2. However, wild-type pRb was able to bind to a region of Id-2 corresponding to only the HLH domain. In vivo, a physical association between Id-2 and pRb was seen in cross-linked extracts from SAOS-2 cells transfected with Id-2 and pRb. Our data identify a role for Id-2 in the regulation of cellular proliferation and suggest that the interaction between Id-2 and pRB is a molecular pathway over which synchronous changes in growth and differentiation are mediated in vivo.
细胞生长和分化通常是相互拮抗的。碱性螺旋-环-螺旋(bHLH)家族的蛋白质与DNA结合,并在特定细胞类型的分化中发挥重要作用。Id蛋白与bHLH转录因子形成异二聚体,阻断它们对谱系特异性基因表达的激活,从而抑制细胞分化。为了研究Id-2对细胞增殖的影响,我们在人骨肉瘤细胞系U2OS中过表达Id-2。U2OS中Id-2的表达降低了生长所需的血清量,并通过缩短倍增时间和增加S期细胞百分比来刺激细胞增殖。我们证明,Id-2的表达能够逆转视网膜母细胞瘤肿瘤抑制基因pRB产物介导的细胞增殖抑制和细胞周期进程阻滞。这种效应与转染细胞中pRb磷酸化状态的变化无关。在体外,细胞裂解物中未磷酸化的pRb特异性结合Id-2,但不能结合缺乏HLH结构域的Id-2突变形式,该突变形式也不能拮抗pRb引起的生长停滞。在E1A/大T结合口袋内含有突变的体外合成pRb不结合Id-2。然而,野生型pRb能够结合Id-2中仅对应于HLH结构域的区域。在体内,在用Id-2和pRb转染的SAOS-2细胞的交联提取物中观察到Id-2和pRb之间的物理关联。我们的数据确定了Id-2在细胞增殖调节中的作用,并表明Id-2和pRB之间的相互作用是体内介导生长和分化同步变化的分子途径。