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Publication : Melanosomal tyrosine transport in normal and pink-eyed dilution murine melanocytes.

First Author  Gahl WA Year  1995
Journal  Pigment Cell Res Volume  8
Issue  5 Pages  229-33
PubMed ID  8789196 Mgi Jnum  J:31367
Mgi Id  MGI:78869 Doi  10.1111/j.1600-0749.1995.tb00668.x
Citation  Gahl WA, et al. (1995) Melanosomal tyrosine transport in normal and pink-eyed dilution murine melanocytes. Pigment Cell Res 8(5):229-33
abstractText  Tyrosine is the endogenous substrate for melanin production within melanosomes, but the method of tyrosine transport into the melanosome has not been investigated. In the mouse, melanogenesis is disrupted by mutations in the p gene resulting in the pink-eyed dilution phenotype; it has been suggested that the p gene codes for a tyrosine transport protein. We determined that normal (melan-a) melanosome-rich granular fractions take up 10 mu m [H- 3]tyrosine at 21.1 +/- 6.1 (SEM, standard error of the mean) pmol/min/ mg protein (N=7) compared with 21.3 +/- 5.8 SEM pmol/min/mg protein (N=5) for pink-eyed dilution, whose plasma membrane tyrosine transport was also normal (K-m 89 mu M; V-max 302 pmol/min/mg cell protein). We also demonstrated that pink-eyed dilution melanosomes are immature by virtue of their low density, high hexosaminidase activity, and lack of pigment. These data indicate that a tyrosine transport system exists in the melanosomal membrane and that the p gene does not encode a tyrosine transporter of critical importance.
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