Weil C F, Oakley C E, Oakley B R
Mol Cell Biol. 1986 Aug;6(8):2963-8. doi: 10.1128/mcb.6.8.2963-2968.1986.
We identified four mutations in two previously undescribed loci involved in microtubule function in Aspergillus nidulans as extragenic suppressors of benA33, a heat-sensitive beta-tubulin mutation. Three of the four mutations map to a locus closely linked to riboB on linkage group VIII; we designated this locus mipA (for microtubule-interacting protein). We were not able to map the remaining suppressor because of chromosomal rearrangements. However, since it recombines with riboB at a significantly higher frequency than the mipA alleles, it is unlikely to be in mipA; thus, we designated it mipB1. The mip mutations are not allelic to the previously identified loci that encode alpha- and beta-tubulin, and it is likely that mipA and mipB encode previously unidentified nontubulin proteins involved in microtubule function. Each of the mip mutations suppresses the heat sensitivity conferred by benA33 and suppresses the blockage of nuclear division and movement conferred by this mutation at high temperatures. Interactions between mipA and benA are allele specific. All of the mipA mutations are cryptic in a wild-type benA background but cause cold sensitivity in combination with benA33. These mutations also confer cold sensitivity in combination with benA31 and benA32 and reduce the resistance conferred by these mutations to the antimicrotubule agent benomyl but do not suppress the heat sensitivity conferred by these alleles. Finally, the mipA alleles suppress the heat sensitivity conferred by benA11, benA17, and benA21 but do not confer cold sensitivity in combination with these alleles.
我们在构巢曲霉中两个先前未描述的与微管功能相关的基因座中鉴定出四个突变,作为benA33(一种热敏感β-微管蛋白突变)的基因外抑制子。这四个突变中的三个定位于与第八连锁群上的riboB紧密连锁的一个基因座;我们将这个基因座命名为mipA(微管相互作用蛋白)。由于染色体重排,我们无法定位其余的抑制子。然而,由于它与riboB的重组频率明显高于mipA等位基因,它不太可能在mipA中;因此,我们将其命名为mipB1。mip突变与先前鉴定的编码α-和β-微管蛋白的基因座不是等位基因,并且mipA和mipB可能编码参与微管功能的先前未鉴定的非微管蛋白。每个mip突变都抑制了benA33赋予的热敏感性,并抑制了该突变在高温下对核分裂和运动的阻断。mipA和benA之间的相互作用是等位基因特异性的。所有mipA突变在野生型benA背景中是隐性的,但与benA33组合时会导致冷敏感性。这些突变与benA31和benA32组合时也会导致冷敏感性,并降低这些突变赋予的对抗微管剂苯菌灵的抗性,但不抑制这些等位基因赋予的热敏感性。最后,mipA等位基因抑制了benA11、benA17和benA21赋予的热敏感性,但与这些等位基因组合时不会导致冷敏感性。