Cellular and ultrastructural characterization of the grey-morph phenotype in southern right whales (Eubalaena australis)

Eroh, G. D., Clayton, F. C., Florell, S. R., Cassidy, P. B., Chirife, A., Maron, C. F., Valenzuela, L. O., Campbell, M. S., Seger, J., Rowntree, V. J., Leachman, S. A. (February 2017) Cellular and ultrastructural characterization of the grey-morph phenotype in southern right whales (Eubalaena australis). PLoS One, 12 (2). e0171449. ISSN 1932-6203

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URL: https://www.ncbi.nlm.nih.gov/pubmed/28170433
DOI: 10.1371/journal.pone.0171449

Abstract

Southern right whales (SRWs, Eubalena australis) are polymorphic for an X-linked pigmentation pattern known as grey morphism. Most SRWs have completely black skin with white patches on their bellies and occasionally on their backs; these patches remain white as the whale ages. Grey morphs (previously referred to as partial albinos) appear mostly white at birth, with a splattering of rounded black marks; but as the whales age, the white skin gradually changes to a brownish grey color. The cellular and developmental bases of grey morphism are not understood. Here we describe cellular and ultrastructural features of grey-morph skin in relation to that of normal, wild-type skin. Melanocytes were identified histologically and counted, and melanosomes were measured using transmission electron microscopy. Grey-morph skin had fewer melanocytes when compared to wild-type skin, suggesting reduced melanocyte survival, migration, or proliferation in these whales. Grey-morph melanocytes had smaller melanosomes relative to wild-type skin, normal transport of melanosomes to surrounding keratinocytes, and normal localization of melanin granules above the keratinocyte nuclei. These findings indicate that SRW grey-morph pigmentation patterns are caused by reduced numbers of melanocytes in the skin, as well as by reduced amounts of melanin production and/or reduced sizes of mature melanosomes. Grey morphism is distinct from piebaldism and albinism found in other species, which are genetic pigmentation conditions resulting from the local absence of melanocytes, or the inability to synthesize melanin, respectively.

Item Type: Paper
Subjects: bioinformatics
bioinformatics > genomics and proteomics > annotation > phenotyping
CSHL Authors:
Communities: CSHL labs > Ware lab
Depositing User: Matt Covey
Date: 7 February 2017
Date Deposited: 16 Feb 2017 17:57
Last Modified: 06 Jul 2021 19:16
PMCID: PMC5295704
Related URLs:
URI: https://repository.cshl.edu/id/eprint/34131

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