A microarray study of altered gene expression during melanoblasts migration in normal pigmented White Leghorn and hyperpigmented mutant Silky Fowl

Yulin LI, Deping HAN, Junying LI, Dawn KOLTES, Xuemei DENG

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Front. Agr. Sci. Eng. ›› 2014, Vol. 1 ›› Issue (4) : 299-306. DOI: 10.15302/J-FASE-2014040
RESEARCH ARTICLE
RESEARCH ARTICLE

A microarray study of altered gene expression during melanoblasts migration in normal pigmented White Leghorn and hyperpigmented mutant Silky Fowl

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Abstract

Melanoblasts originating from neural crest cells can migrate through the mesenchyme of the developed embryo and give rise to melanocytes. Unlike the melanocytes that are confined to the integument in other vertebrates, melanocytes in Silky Fowl can reach the ventral regions of the embryos owing to differences in gene expression in the process of melanoblasts migration. In this study, we used microarray profiling to identify differences in gene expression between White Leghorn and Silky Fowl. Differential expression of 2517 microarray probes (P<0.01, Fold Change>2) was observed in Silky Fowl compared to White Leghorn. After filtration by cluster analysis, functional annotation and pathway analysis, eight differentially expressed genes were identified to be closely related to the development of melanocytes. Moreover, differences in expression of immune genes were also detected between Silky Fowl and White Leghorn. The differentially expressed genes associated with melanocyte development were verified by q-PCR, and results were highly consistent with the microarray data. The genes with significantly altered expression involved in melanoblast migration and development suggested that different microenvironments resulted in the abnormal melanoblast migration in Silky Fowl, although there were no big differences in melanoblast development between these two breeds. The candidate genes discovered in this study are beneficial to understand the molecular mechanism of hyperpigmentation in Silky Fowl.

Keywords

Silky Fowl / White Leghorn / melanoblast migration / gene expression

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Yulin LI, Deping HAN, Junying LI, Dawn KOLTES, Xuemei DENG. A microarray study of altered gene expression during melanoblasts migration in normal pigmented White Leghorn and hyperpigmented mutant Silky Fowl. Front. Agr. Sci. Eng., 2014, 1(4): 299‒306 https://doi.org/10.15302/J-FASE-2014040

References

[1]
Loring J F, Erickson C A. Neural crest cell migratory pathways in the trunk of the chick embryo. Developmental Biology, 1987, 121(1): 220–236
CrossRef Pubmed Google scholar
[2]
Dorsky R I, Moon R T, Raible D W. Control of neural crest cell fate by the Wnt signalling pathway. Nature, 1998, 396(6709): 370–373
CrossRef Pubmed Google scholar
[3]
Jin E J, Erickson C A, Takada S, Burrus L W. Wnt and BMP signaling govern lineage segregation of melanocytes in the avian embryo. Developmental Biology, 2001, 233(1): 22–37
CrossRef Pubmed Google scholar
[4]
Harris M L, Erickson C A. Lineage specification in neural crest cell pathfinding. Developmental Dynamics, 2007, 236(1): 1–19
CrossRef Pubmed Google scholar
[5]
Faraco C D, Vaz S A, Pástor M V, Erickson C A. Hyperpigmentation in the Silkie fowl correlates with abnormal migration of fate-restricted melanoblasts and loss of environmental barrier molecules. Developmental Dynamics, 2001, 220(3): 212–225
CrossRef Pubmed Google scholar
[6]
Ma Y, Li A, Faller W J, Libertini S, Fiorito F, Gillespie D A, Sansom O J, Yamashiro S, Machesky L M. Fascin 1 is transiently expressed in mouse melanoblasts during development and promotes migration and proliferation. Development, 2013, 140(10): 2203–2211
CrossRef Pubmed Google scholar
[7]
Lindsay C R, Lawn S, Campbell A D, Faller W J, Rambow F, Mort R L, Timpson P, Li A, Cammareri P, Ridgway R A, Morton J P, Doyle B, Hegarty S, Rafferty M, Murphy I G, McDermott E W, Sheahan K, Pedone K, Finn A J, Groben P A, Thomas N E, Hao H, Carson C, Norman J C, Machesky L M, Gallagher W M, Jackson I J, Van Kempen L, Beermann F, Der C, Larue L, Welch H C, Ozanne B W, Sansom O J. P-Rex1 is required for efficient melanoblast migration and melanoma metastasis. Nature Communications, 2011, 2: 555
CrossRef Pubmed Google scholar
[8]
Santiago A, Erickson C A. Ephrin-B ligands play a dual role in the control of neural crest cell migration. Development, 2002, 129(15): 3621–3632
Pubmed
[9]
Jia L, Cheng L, Raper J. Slit/Robo signaling is necessary to confine early neural crest cells to the ventral migratory pathway in the trunk. Developmental Biology, 2005, 282(2): 411–421
CrossRef Pubmed Google scholar
[10]
Pla P, Alberti C, Solov’eva O, Pasdar M, Kunisada T, Larue L. Ednrb2 orients cell migration towards the dorsolateral neural crest pathway and promotes melanocyte differentiation. Pigment Cell Research, 2005, 18(3): 181–187
CrossRef Pubmed Google scholar
[11]
Muroya S, Tanabe R, Nakajima I, Chikuni K. Molecular characteristics and site specific distribution of the pigment of the Silky fowl. Journal of Veterinary Medical Science, 2000, 62(4): 391–395
CrossRef Pubmed Google scholar
[12]
Reedy M V, Faraco C D, Erickson C A. Specification and migration of melanoblasts at the vagal level and in hyperpigmented Silkie chickens. Developmental Dynamics, 1998, 213(4): 476–485
CrossRef Pubmed Google scholar
[13]
de Freitas P F, Ferreira F F, Faraco C D. PNA-positive glycoconjugates are negatively correlated with the access of neural crest cells to the gut in chicken embryos. The Anatomical Record. Part A: Discoveries in Molecular, Cellular, and Evolutionary Biology, 2003, 273A(2): 705–713
CrossRef Pubmed Google scholar
[14]
Dorshorst B, Okimoto R, Ashwell C. Genomic regions associated with dermal hyperpigmentation, polydactyly and other morphological traits in the Silkie chicken. Journal of Heredity, 2010, 101(3): 339–350
CrossRef Pubmed Google scholar
[15]
Shinomiya A, Kayashima Y, Kinoshita K, Mizutani M, Namikawa T, Matsuda Y, Akiyama T. Gene duplication of endothelin 3 is closely correlated with the hyperpigmentation of the internal organs (Fibromelanosis) in Silky chickens. Genetics, 2012, 190(2): 627–638
CrossRef Pubmed Google scholar
[16]
Li X, Chiang H I, Zhu J, Dowd S E, Zhou H. Characterization of a newly developed chicken 44K Agilent microarray. BMC Genomics, 2008, 9(1): 60
CrossRef Pubmed Google scholar
[17]
Li Y, Zhu X, Yang L, Li J, Lian Z, Li N, Deng X. Expression and network analysis of genes related to melanocyte development in the Silky Fowl and White Leghorn embryos. Molecular Biology Reports, 2011, 38(2): 1433–1441
CrossRef Pubmed Google scholar
[18]
Shippy R, Sendera T J, Lockner R, Palaniappan C, Kaysser-Kranich T, Watts G, Alsobrook J. Performance evaluation of commercial short-oligonucleotide microarrays and the impact of noise in making cross-platform correlations. BMC Genomics, 2004, 5(1): 61
CrossRef Pubmed Google scholar
[19]
Sarson A J, Wang Y, Kang Z, Dowd S E, Lu Y, Yu H, Han Y, Zhou H, Gong J. Gene expression profiling within the spleen of Clostridium perfringens-challenged broilers fed antibiotic-medicated and non-medicated diets. BMC Genomics, 2009, 10(1): 260
CrossRef Pubmed Google scholar
[20]
Kendziorski C M, Zhang Y, Lan H, Attie A D. The efficiency of pooling mRNA in microarray experiments. Biostatistics, 2003, 4(3): 465–477
CrossRef Pubmed Google scholar
[21]
Peng X, Wood C L, Blalock E M, Chen K C, Landfield P W, Stromberg A J. Statistical implications of pooling RNA samples for microarray experiments. BMC Bioinformatics, 2003, 4(1): 26
CrossRef Pubmed Google scholar
[22]
Bonaventure J, Domingues M J, Larue L. Cellular and molecular mechanisms controlling the migration of melanocytes and melanoma cells. Pigment Cell & Melanoma Research, 2013, 26(3): 316–325
CrossRef Pubmed Google scholar
[23]
Wehrle-Haller B, Morrison-Graham K, Weston J A. Ectopic c-kit expression affects the fate of melanocyte precursors in Patch mutant embryos. Developmental Biology, 1996, 177(2): 463–474
CrossRef Pubmed Google scholar
[24]
Reedy M V, Johnson R L, Erickson C A. The expression patterns of c-kit and S1 in chicken embryos suggest unexpected roles for these genes in somite and limb development. Gene Expression Patterns, 2003, 3(1): 53–58
CrossRef Pubmed Google scholar
[25]
Pla P, Larue L. Involvement of endothelin receptors in normal and pathological development of neural crest cells. International Journal of Developmental Biology, 2003, 47(5): 315–325
Pubmed
[26]
Nataf V, Amemiya A, Yanagisawa M, Le Douarin N M. The expression pattern of endothelin 3 in the avian embryo. Mechanisms of Development, 1998, 73(2): 217–220
CrossRef Pubmed Google scholar
[27]
Lahav R, Dupin E, Lecoin L, Glavieux C, Champeval D, Ziller C, Le Douarin N M. Endothelin 3 selectively promotes survival and proliferation of neural crest-derived glial and melanocytic precursors in vitro. Proceedings of the National Academy of Sciences of the United States of America, 1998, 95(24): 14214–14219
CrossRef Pubmed Google scholar
[28]
Seidah N G, Benjannet S, Hamelin J, Mamarbachi A M, Basak A, Marcinkiewicz J, Mbikay M, Chrétien M, Marcinkiewicz M. The subtilisin/kexin family of precursor convertases. Emphasis on PC1, PC2/7B2, POMC and the novel enzyme SKI-1. Annals of the New York Academy of Sciences, 1999, 885(1): 57–74
CrossRef Pubmed Google scholar
[29]
Suzuki I, Cone R D, Im S, Nordlund J, Abdel-Malek Z A. Binding of melanotropic hormones to the melanocortin receptor MC1R on human melanocytes stimulates proliferation and melanogenesis. Endocrinology, 1996, 137(5): 1627–1633
Pubmed
[30]
Kauser S, Thody A J, Schallreuter K U, Gummer C L, Tobin D J. A fully functional proopiomelanocortin/melanocortin-1 receptor system regulates the differentiation of human scalp hair follicle melanocytes. Endocrinology, 2005, 146(2): 532–543
CrossRef Pubmed Google scholar
[31]
Takeuchi S, Teshigawara K, Takahashi S. Widespread expression of Agouti-related protein (AGRP) in the chicken: a possible involvement of AGRP in regulating peripheral melanocortin systems in the chicken. Biochimica et Biophysica Acta, 2000, 1496(2–3): 261– 269
CrossRef Pubmed Google scholar
[32]
Berson J F, Theos A C, Harper D C, Tenza D, Raposo G, Marks M S. Proprotein convertase cleavage liberates a fibrillogenic fragment of a resident glycoprotein to initiate melanosome biogenesis. Journal of Cell Biology, 2003, 161(3): 521–533
CrossRef Pubmed Google scholar
[33]
Lamoreux M L, Wakamatsu K, Ito S. Interaction of major coat color gene functions in mice as studied by chemical analysis of eumelanin and pheomelanin. Pigment Cell Research, 2001, 14(1): 23–31
CrossRef Pubmed Google scholar
[34]
García-Borrón J C, Solano F. Molecular anatomy of tyrosinase and its related proteins: beyond the histidine-bound metal catalytic center. Pigment Cell Research, 2002, 15(3): 162–173
CrossRef Pubmed Google scholar

Acknowledgements

This work was supported by Natural Science Foundation of China (31472082, 30771535) and the National High-tech R&D Program of China (2013AA102501).
Compliance with ethics guidelinesƒYulin Li, Deping Han, Junying Li, Dawn Koltes and Xuemei Deng declare that they have no conflict of interest or financial conflicts to disclose.ƒAll applicable institutional and national guidelines for the care and use of animals were followed.

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Higher Education Press and Springer-Verlag Berlin Heidelberg
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