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参与紫球海胆母体mRNA定位的反式作用因子的分离。

Isolation of a trans-acting factor involved in localization of Paracentrotus lividus maternal mRNAs.

作者信息

Costa C, Romancino D P, Ingrassia A, Vizzini A, Di Carlo M

机构信息

Istituto di Biologia dello Sviluppo CNR, Palermo, Italy.

出版信息

RNA. 1999 Oct;5(10):1290-8. doi: 10.1017/s1355838299982171.

Abstract

Localization of Paracentrotus lividus bep maternal mRNAs at the animal pole occurs by association with the cytoskeleton and involves a 54-kDa protein, called LP54, that is able to bind to the 3' untranslated regions (UTRs) of bep mRNAs. We describe here the isolation and purification of this protein. Antibodies raised against purified LP54 allowed us to establish its localization in P. lividus eggs and embryos. This localization coincides with the mRNAs with which it is associated, that is, the animal pole in the egg, and, after fertilization, the regions derived from this part of the egg, and finally the oral ectoderm of the pluteus. Association with the cytoskeleton was shown by the copurification of LP54 in a microtubule preparation. Involvement in bep mRNA localization was demonstrated by microinjection of anti-LP54 antibodies in P. lividus eggs, which caused alteration of spatial distribution of bep3 mRNA.

摘要

紫球海胆bep母体mRNA在动物极的定位是通过与细胞骨架结合实现的,涉及一种名为LP54的54 kDa蛋白质,它能够与bep mRNA的3'非翻译区(UTR)结合。我们在此描述该蛋白质的分离和纯化。针对纯化的LP54产生的抗体使我们能够确定其在紫球海胆卵和胚胎中的定位。这种定位与它所关联的mRNA一致,即在卵中的动物极,受精后,来自卵这一部分的区域,最终是长腕幼虫的口外胚层。在微管制剂中LP54的共纯化显示了它与细胞骨架的结合。通过向紫球海胆卵中显微注射抗LP54抗体,导致bep3 mRNA空间分布改变,证明了其参与bep mRNA的定位。

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