Identification of mRNA-binding proteins during development characterization of Bufo arenarum cellular nucleic acid binding protein

CALCATERRA, NORA B; PALATNIK, JAVIER; BUSTOS, DIEGO M; ARRANZ, SILVIA E; CABADA, MARCELO O

DEVELOPMENT GROWTH & DIFFERENTIATION

Año: 1999 vol. 41 p. 183 - 191

0012-1592

Ultraviolet irradiation was used to covalently cross-link poly(A)1RNA and associated proteins in eggs and embryos of the toad Bufo arenarum. Four major proteins with apparent sizes of 60, 57, 45 and 30–24 kDa were identified. It was observed that the same mRNA-binding proteins were isolated from eggs to gastrula and neural stages of development. The 30 kDa polypeptide, p30, appeared as the main ultraviolet (UV) cross-linked protein in the developmental stages analyzed. By means of polyclonal antibodies, it was determined that this polypeptide has a cytoplasmic localization and it was detected in liver, eggs and embryos. The presence of p30 was also analyzed by western blot during oogenesis and development. The 30 kDa polypeptide was present in all stages analyzed but it could not be detected in stages I–II of oogenesis. At the neural stage, the relative amount of p30 began to decrease, reaching its lowest levels after stages 26–30 (tail-bud in Bufo arenarum). On the basis of purification, immunoprecipitation and western blot assays the 30 kDa protein was identified as the Bufo arenarumcellular nucleic acid binding protein. embryos of the toad Bufo arenarum. Four major proteins with apparent sizes of 60, 57, 45 and 30–24 kDa were identified. It was observed that the same mRNA-binding proteins were isolated from eggs to gastrula and neural stages of development. The 30 kDa polypeptide, p30, appeared as the main ultraviolet (UV) cross-linked protein in the developmental stages analyzed. By means of polyclonal antibodies, it was determined that this polypeptide has a cytoplasmic localization and it was detected in liver, eggs and embryos. The presence of p30 was also analyzed by western blot during oogenesis and development. The 30 kDa polypeptide was present in all stages analyzed but it could not be detected in stages I–II of oogenesis. At the neural stage, the relative amount of p30 began to decrease, reaching its lowest levels after stages 26–30 (tail-bud in Bufo arenarum). On the basis of purification, immunoprecipitation and western blot assays the 30 kDa protein was identified as the Bufo arenarumcellular nucleic acid binding protein. 1RNA and associated proteins in eggs and embryos of the toad Bufo arenarum. Four major proteins with apparent sizes of 60, 57, 45 and 30–24 kDa were identified. It was observed that the same mRNA-binding proteins were isolated from eggs to gastrula and neural stages of development. The 30 kDa polypeptide, p30, appeared as the main ultraviolet (UV) cross-linked protein in the developmental stages analyzed. By means of polyclonal antibodies, it was determined that this polypeptide has a cytoplasmic localization and it was detected in liver, eggs and embryos. The presence of p30 was also analyzed by western blot during oogenesis and development. The 30 kDa polypeptide was present in all stages analyzed but it could not be detected in stages I–II of oogenesis. At the neural stage, the relative amount of p30 began to decrease, reaching its lowest levels after stages 26–30 (tail-bud in Bufo arenarum). On the basis of purification, immunoprecipitation and western blot assays the 30 kDa protein was identified as the Bufo arenarumcellular nucleic acid binding protein.