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Fission yeast tmsl protein abrogates normal development in Xenopus laevis embryos.

作者信息

Wagner Peter, Hoever Michael, Appel Katrin, Knöchel Walter, Montenarh Mathias

机构信息

Medizinische Biochemie, Universität des Saarlandes, Gebdude 44, D-66421, Homburg/Saar, Germany.

Abteilung Biochemie, Universität Ulm, Albert Einstein Allee 11, D-89069, Ulm, Germany.

出版信息

Rouxs Arch Dev Biol. 1995 Jan;204(3):198-202. doi: 10.1007/BF00241273.

Abstract

Recently we cloned tms1 (a putative dehydrogenase) by complementation of a human tumour-derived mutant p53 induced growth arrest in fission yeast. Microinjection of purified tmsl protein into Xenopus laevis embryos abrogated normal embryo development by causing cleavage retardation or cleavage arrest of injected blastomeres in a concentration dependant manner, whereas injection of specific affinity purified tms1 antiserum showed no significant morphological defects. Microinjection of tms1 protein together with affinity purified tms1 antibody resulted in a significantly reduced number of cleavage arrested embryos.

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