Stirling D A, Rayner T F, Prescott A R, Stark M J
Department of Biochemistry, The University, Dundee, UK.
J Cell Sci. 1996 Jun;109 ( Pt 6):1297-310. doi: 10.1242/jcs.109.6.1297.
We have generated three temperature-sensitive alleles of SPC110, which encodes the 110 kDa component of the yeast spindle pole body (SPB). Each of these alleles carries point mutations within the calmodulin (CaM) binding site of Spc110p which affect CaM binding in vitro; two of the mutant proteins fail to bind CaM detectably (spc110-111, spc110-118) while binding to the third (spc110-124) is temperature-sensitive. All three alleles are suppressed to a greater or lesser extent by elevated dosage of the CaM gene (CMD1), suggesting that disruption of CaM binding is the primary defect in each instance. To determine the consequences on Spc110p function of loss of effective CaM binding, we have therefore examined in detail the progression of synchronous cultures through the cell division cycle at the restrictive temperature. In each case, cells replicate their DNA but then lose viability. In spc110-124, most cells duplicate and partially separate the SPBs but fail to generate a functional mitotic spindle, a phenotype which we term 'abnormal metaphase'. Conversely, spc110-111 cells initially produce nuclear microtubules which appear well-organised but on entry into mitosis accumulate cells with 'broken spindles', where one SPB has become completely detached from the nuclear DNA. In both cases, the bulk of the cells suffer a lethal failure to segregate the DNA.
我们构建了SPC110的三个温度敏感等位基因,该基因编码酵母纺锤体极体(SPB)的110 kDa组分。这些等位基因中的每一个都在Spc110p的钙调蛋白(CaM)结合位点内携带点突变,这些突变在体外影响CaM结合;其中两个突变蛋白无法检测到与CaM结合(spc110 - 111、spc110 - 118),而与第三个(spc110 - 124)的结合是温度敏感的。通过提高CaM基因(CMD1)的剂量,这三个等位基因都或多或少地受到了抑制,这表明CaM结合的破坏是每种情况下的主要缺陷。为了确定有效CaM结合丧失对Spc110p功能的影响,我们详细研究了同步培养物在限制温度下通过细胞分裂周期的进程。在每种情况下,细胞都能复制其DNA,但随后失去活力。在spc110 - 124中,大多数细胞复制并部分分离了SPB,但未能形成功能性有丝分裂纺锤体,这种表型我们称为“异常中期”。相反,spc110 - 111细胞最初产生看起来组织良好的核微管,但进入有丝分裂时会积累带有“断裂纺锤体”的细胞,其中一个SPB已完全与核DNA分离。在这两种情况下,大多数细胞都因DNA分离失败而致死。