Premium
Subcellular Distribution of Thymosin β 4
Author(s) -
ZOUBEK ROBERT E.,
HANNAPPEL EWALD
Publication year - 2007
Publication title -
annals of the new york academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.712
H-Index - 248
eISSN - 1749-6632
pISSN - 0077-8923
DOI - 10.1196/annals.1415.031
Subject(s) - cytoplasm , thymosin , nucleus , chemistry , lysine , microbiology and biotechnology , cadaverine , biochemistry , biology , amino acid , spermine , enzyme
: The localization of Oregon Green cadaverine‐labeled thymosin β 4 , its fragments, and variants was investigated in cytoplasm‐depleted A431 cells and in microinjected cells without and with fixation. The studied thymosin β 4 variants included substitutions of the lysine residues within the basic cluster (14‐KSKLKK‐19) and the actin‐binding motif (17‐LKKTETQ‐23). In contrast to Oregon Green cadaverine, none of the variants or fragments of thymosin β 4 could pass the intact nuclear pore of cytoplasm‐depleted cells and were hence excluded from the nucleus. However, an equal distribution of all thymosin β 4 variants was observed in living cells. The nuclear localization is neither dependent on the actin‐binding ability of thymosin β 4 nor on its basic lysine cluster. The equal distribution of the β‐thymosins, the ability of the fragments thymosin β 4 1 − 26 and β 4 27 − 43 to enter the nucleus in intact cells immediately after injection, and their exclusion from cytoplasm‐depleted nuclei make it unlikely that they are transported by a single transport protein. A passive but regulated diffusion could explain the described ability of thymosin β 4 to shuttle into the nucleus.