Loss of cellular motor protein contributes to tumor formation

2006 ◽  
1999 ◽  
Vol 73 (12) ◽  
pp. 10508-10513 ◽  
Author(s):  
Yao Tang ◽  
Ulrike Winkler ◽  
Eric O. Freed ◽  
Ted A. Torrey ◽  
Wankee Kim ◽  
...  

ABSTRACT Previously we demonstrated that murine retroviral Gag proteins associate with a cellular motor protein, KIF-4. Using the yeast two-hybrid assay, we also found an association of KIF-4 with Gag proteins of Mason-Pfizer monkey virus (MPMV), simian immunodeficiency virus (SIV), and human immunodeficiency virus type 1 (HIV-1). Studies performed with mammalian cell systems confirmed that the HIV-1 Gag protein associates with KIF-4. Soluble cytoplasmic proteins from cells infected with recombinant vaccinia virus expressing the entire Gag-Pol precursor protein of HIV-1 or transfected with HIV-1 molecular clone pNL4-3 were fractionated by sucrose gradient centrifugation and further separated by size-exclusion and anion-exchange chromatographies. KIF-4 and HIV-1 Gag cofractionated in both chromatographic separations. Immunoprecipitation assays have also verified the KIF-4–Gag association. KIF-4 binds mainly to the Gag precursor (Pr55 Gag) and a matrix-capsid processing intermediate (Pr42) but not to other processed Gag products. The binding of Gag is mediated by a domain of KIF-4 proximal to the C terminus. These results, and our previous studies, raise the possibility that KIF-4 may play an important role in retrovirus Gag protein transport.


2006 ◽  
Vol 16 (15) ◽  
pp. 1559-1564 ◽  
Author(s):  
Manjari Mazumdar ◽  
Ji-Hyeon Lee ◽  
Kundan Sengupta ◽  
Thomas Ried ◽  
Sushil Rane ◽  
...  

2015 ◽  
Vol 46 (S 01) ◽  
Author(s):  
O. Schwartz ◽  
N. Loges ◽  
J. Wallmeier ◽  
G. Dougherty ◽  
P. Pennekamp ◽  
...  

2016 ◽  
Vol 136 (9) ◽  
pp. 384-389
Author(s):  
Kazuya Fujimoto ◽  
Hirofumi Shintaku ◽  
Hidetoshi Kotera ◽  
Ryuji Yokokawa

2020 ◽  
Vol 13 (3) ◽  
pp. 585-591
Author(s):  
Luana Melo ◽  
Isabel Velasco ◽  
Julia Aquino ◽  
Rosangela Rodrigues ◽  
Edris Lopes ◽  
...  

Fibropapillomatosis is a neoplastic disease that affects sea turtles. It is characterized by multiple papillomas, fibropapillomas and cutaneous and/or visceral fibromas. Although its etiology has not been fully elucidated, it is known that there is a strong involvement of an alpha - herpesvirus, but the influence of other factors such as parasites, genetics, chemical carcinogens, contaminants, immunosuppression and ultraviolet radiation may be important in the disease, being pointed out as one of the main causes of a reduction in the green turtle population. Thus, the objective of this article was to describe the morphology of cutaneous fibropapillomas found in specimens of the green turtle (Chelonia mydas), using light and scanning electron microscopy in order to contribute to the mechanism of tumor formation. Microscopically, it presented hyperplastic stromal proliferation and epidermal proliferation with hyperkeratosis. The bulky mass was coated with keratin, with some keratinocyte invaginations, that allowed the keratin to infiltrate from the epidermis into the dermis, forming large keratinized circular spirals. Another fact that we observed was the influence of the inflammation of the tumors caused by ectoparasites.


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