Facultad de Química, Departamento de Bioquímica, UNAM, Avenida Universidad y Copilco, México DF 04510, México.
I. Medizinische Klinik and Poliklinik, Universitätsmedizin der Johannes Gutenberg-Universität Mainz Obere Zahlbacherstr. 63 55131 Mainz, Germany.
J Exp Bot. 2017 Mar 1;68(7):1585-1597. doi: 10.1093/jxb/erx054.
The family of maize Kip-related proteins (KRPs) has been studied and a nomenclature based on the relationship to rice KRP genes is proposed. Expression studies of KRP genes indicate that all are expressed at 24 h of seed germination but expression is differential in the different tissues of maize plantlets. Recombinant KRP1;1 and KRP4;2 proteins, members of different KRP classes, were used to study association to and inhibitory activity on different maize cyclin D (CycD)-cyclin-dependent kinase (CDK) complexes. Kinase activity in CycD2;2-CDK, CycD4;2-CDK, and CycD5;3-CDK complexes was inhibited by both KRPs; however, only KRP1;1 inhibited activity in the CycD6;1-CDK complex, not KRP4;2. Whereas KRP1;1 associated with either CycD2;2 or CycD6;1, and to cyclin-dependent kinase A (CDKA) recombinant proteins, forming ternary complexes, KRP4;2 bound CDKA and CycD2;2 but did not bind CycD6;1, establishing a differential association capacity. All CycD-CDK complexes included here phosphorylated both the retinoblastoma-related (RBR) protein and the two KRPs; interestingly, while KRP4;2 phosphorylated by the CycD2;2-CDK complex increased its inhibitory capacity, when phosphorylated by the CycD6;1-CDK complex the inhibitory capacity was reduced or eliminated. Evidence suggests that the phosphorylated residues in KRP4;2 may be different for every kinase, and this would influence its performance as a cyclin-CDK inhibitor.
玉米 Kip 相关蛋白(KRPs)家族已被研究,并提出了基于与水稻 KRP 基因关系的命名法。KRP 基因的表达研究表明,所有基因在种子萌发 24 小时时均有表达,但在玉米幼苗的不同组织中表达存在差异。不同 KRPs 类别的成员重组 KRP1;1 和 KRP4;2 蛋白被用于研究与不同玉米细胞周期蛋白 D(CycD)-细胞周期蛋白依赖性激酶(CDK)复合物的关联和抑制活性。CycD2;2-CDK、CycD4;2-CDK 和 CycD5;3-CDK 复合物中的激酶活性被两种 KRPs 抑制;然而,只有 KRP1;1 抑制 CycD6;1-CDK 复合物的活性,而 KRP4;2 则不抑制。虽然 KRP1;1 与 CycD2;2 或 CycD6;1 以及细胞周期蛋白依赖性激酶 A(CDKA)重组蛋白结合,形成三元复合物,但 KRP4;2 与 CDKA 和 CycD2;2 结合,但不与 CycD6;1 结合,建立了不同的结合能力。此处包括的所有 CycD-CDK 复合物均磷酸化视网膜母细胞瘤相关(RBR)蛋白和两种 KRPs;有趣的是,当 KRP4;2 被 CycD2;2-CDK 复合物磷酸化时,其抑制能力增加,而当 KRP4;2 被 CycD6;1-CDK 复合物磷酸化时,其抑制能力降低或消除。有证据表明,KRP4;2 中磷酸化残基可能因每种激酶而异,这将影响其作为细胞周期蛋白-CDK 抑制剂的性能。