The DOI matches its Crossref record; 38 of the 38 references it cites were found in a registry or an index.
Melanocyte development in vivo and in neural crest cell cultures: crucial dependence on the Mitf basic-helix-loop-helix-zipper transcription factor
Abstract
The more than 20 different Mitf mutations in the mouse are all associated with deficiencies in neural crest-derived melanocytes that range from minor functional distur-bances with some alleles to complete absence of mature melanocytes with others. In the trunk region of wild-type embryos, Mitf-expressing cells that coexpressed the melanoblast marker Dct and the tyrosine kinase receptor Kit were found in the dorsolateral neural crest migration pathway. In contrast, in embryos homozygous for an Mitf allele encoding a non-functional Mitf protein, Mitf-express-ing cells were extremely rare, no Dct expression was ever found, and the number of Kit-expressing cells was much reduced. Wild-type neural crest cell cultures rapidly gave rise to cells that expressed Mitf and coexpressed Kit and Dct. With time in culture, Kit expression was increased, and pigmented, dendritic cells developed. Addition of the Kit ligand Mgf or endothelin 3 or a combination of these factors all rapidly increased the number of Dct-positive cells. Cultures from Mitf mutant embryos initially displayed Mitf-positive cells similar in numbers and Kit-expression as did wild-type cultures. However, Kit expression did not increase with time in culture and the mutant cells never responded to Mgf or endothelin 3, did not express Dct, and never showed pigment. In fact, even Mitf expression was rapidly lost. The results suggest that Mitf first plays a role in promoting the transition of precursor cells to melanoblasts and subsequently, by influ-encing Kit expression, melanoblast survival.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Le Douarin, N., & Kalcheim, C. (1999) · Cambridge University Press eBooks · doi:10.1017/cbo9780511897948 · Cited by 3,014
Genetic variants and strains of the laboratory mouse
(1990) · Choice Reviews Online · doi:10.5860/choice.28-1324 · Cited by 1,483
The dominant-white spotting (W) locus of the mouse encodes the c-kit proto-oncogene
Geissler, E. N., Ryan, M. A., & Housman, D. E. (1988) · Cell · doi:10.1016/0092-8674(88)90020-7 · Cited by 1,287
Hodgkinson, C. A., Moore, K. J., Nakayama, A., Steingrímsson, E., Copeland, N. G., Jenkins, N. A., & Arnheiter, H. (1993) · Cell · doi:10.1016/0092-8674(93)90429-t · Cited by 1,094
Self-citationConversion of Xenopus Ectoderm into Neurons by NeuroD, a Basic Helix-Loop-Helix Protein
Lee, J. E., Hollenberg, S. M., Snider, L., Turner, D. L., Lipnick, N., & Weintraub, H. (1995) · Science · doi:10.1126/science.7754368 · Cited by 1,023
Hosoda, K., Hammer, R. E., Richardson, J. A., Baynash, A. G., Cheung, J. C., Giaid, A., & Yanagisawa, M. (1994) · Cell · doi:10.1016/0092-8674(94)90017-5 · Cited by 1,005
Baynash, A. G., Hosoda, K., Giaid, A., Richardson, J. A., Emoto, N., Hammer, R. E., & Yanagisawa, M. (1994) · Cell · doi:10.1016/0092-8674(94)90018-3 · Cited by 942
Hemesath, T. J., Steingrímsson, E., McGill, G., Hansen, M. J., Vaught, J., Hodgkinson, C. A., Arnheiter, H., Copeland, N. G., Jenkins, N. A., & Fisher, D. E. (1994) · Genes & Development · doi:10.1101/gad.8.22.2770 · Cited by 673
Self-citationWaardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene
Tassabehji, M., Newton, V. E., & Read, A. P. (1994) · Nature Genetics · doi:10.1038/ng1194-251 · Cited by 666
Copeland, N. G., Gilbert, D. J., Cho, B. C., Donovan, P. J., Jenkins, N. A., Cosman, D., Anderson, D., Lyman, S. D., & Williams, D. E. (1990) · Cell · doi:10.1016/0092-8674(90)90298-s · Cited by 610
Cited by
Lister, J. A., Robertson, C. P., Lepage, T., Johnson, S. L., & Raible, D. W. (1999) · Development · doi:10.1242/dev.126.17.3757 · Cited by 819
Mitf regulation of Dia1 controls melanoma proliferation and invasiveness
Carreira, S., Goodall, J., Denat, L., Rodriguez, M., Nuciforo, P., Hoek, K. S., Testori, A., Larue, L., & Goding, C. R. (2006) · Genes & Development · doi:10.1101/gad.406406 · Cited by 608
Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates
Dutton, K. A., Pauliny, A., Lopes, S. S., Elworthy, S., Carney, T. J., Rauch, J., Geisler, R., Haffter, P., & Kelsh, R. N. (2001) · Development · doi:10.1242/dev.128.21.4113 · Cited by 511
Goding, C. R., & Arnheiter, H. (2019) · Genes & Development · doi:10.1101/gad.324657.119 · Cited by 430
Self-citation“Transcription physiology” of pigment formation in melanocytes: central role of MITF
Vachtenheim, J., & Borovanský, J. (2010) · Experimental Dermatology · doi:10.1111/j.1600-0625.2009.01053.x · Cited by 398
Parichy, D. M., Ransom, D. G., Paw, B., Zon, L. I., & Johnson, S. L. (2000) · Development · doi:10.1242/dev.127.14.3031 · Cited by 384
Lineage-specific requirements of β-catenin in neural crest development
Hari, L., Brault, V., Kléber, M., Lee, H.-Y., Ille, F., Leimeroth, R., Paratore, C., Suter, U., Kemler, R., & Sommer, L. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200209039 · Cited by 320
Dorsky, R. I., Raible, D. W., & Moon, R. T. (2000) · Genes & Development · doi:10.1101/gad.14.2.158 · Cited by 279
The making of a melanocyte: the specification of melanoblasts from the neural crest
Thomas, A. J., & Erickson, C. A. (2008) · Pigment Cell & Melanoma Research · doi:10.1111/j.1755-148x.2008.00506.x · Cited by 253
Parichy, D. M., Mellgren, E. M., Rawls, J. F., Lopes, S. S., Kelsh, R. N., & Johnson, S. L. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9899 · Cited by 230
Interplay between Foxd3 and Mitf regulates cell fate plasticity in the zebrafish neural crest
Curran, K., Lister, J. A., Kunkel, G. R., Prendergast, A., Parichy, D. M., & Raible, D. W. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.04.023 · Cited by 170
Elworthy, S., Lister, J. A., Carney, T. J., Raible, D. W., & Kelsh, R. N. (2003) · Development · doi:10.1242/dev.00461 · Cited by 168
How the zebrafish gets its stripes
Rawls, J. F., Mellgren, E. M., & Johnson, S. L. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0418 · Cited by 165
Leukocyte Tyrosine Kinase Functions in Pigment Cell Development
Lopes, S. S., Yang, X., Müller, J., Carney, T. J., McAdow, A. R., Rauch, G.-J., Jacoby, A. S., Hurst, L. D., Delfino-Machín, M., Haffter, P., et al. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000026 · Cited by 163
Zebrafish Pigment Pattern Formation: Insights into the Development and Evolution of Adult Form
Patterson, L. B., & Parichy, D. M. (2019) · Annual Review of Genetics · doi:10.1146/annurev-genet-112618-043741 · Cited by 151
Assembly of the cnidarian camera-type eye from vertebrate-like components
Kozmik, Z., Ruzickova, J., Jonasova, K., Matsumoto, Y., Vopalensky, P., Kozmikova, I., Strnad, H., Kawamura, S., Piatigorsky, J., Paces, V., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800388105 · Cited by 147
Johnson, S. L., Nguyen, A. N., & Lister, J. A. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2010.12.004 · Cited by 85
(2002) · PubMed · Cited by 79
Jivanji, S., Worth, G., Lopdell, T. J., Yeates, A., Couldrey, C., Reynolds, E., Tiplady, K., McNaughton, L., Johnson, T. J. J., Davis, S. R., et al. (2019) · Genetics Selection Evolution · doi:10.1186/s12711-019-0506-2 · Cited by 41
An ongoing role for Wnt signaling in differentiating melanocytes in vivo
Vibert, L., Aquino, G., Gehring, I., Subkankulova, T., Schilling, T. F., Rocco, A., & Kelsh, R. N. (2017) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.12568 · Cited by 35
Bian, F., Yang, X., Ou, Z., Luo, J., Tan, B., Yuan, M., Chen, T., & Yang, R. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00698 · Cited by 22
Metadata
- Authors
- Opdecamp, K., Nakayama, A., Nguyen, M.-T. T., Hodgkinson, C. A., Pavan, W. J., & Arnheiter, H.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 1997-06-15
- Volume
- 124
- Issue
- 12
- Pages
- 2377-2386
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2130987003
- Cited by
- 299
- References
- 38
- FWCI
- 5.68
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.