Techniques and probes for the study of Xenopus tropicalis development

• Published in: Developmental dynamics Vol. 225; no. 4; pp. 499 - 510
• Main Authors: Khokha, Mustafa K., Chung, Christina, Bustamante, Erika L., Gaw, Lisa W.K., Trott, Kristin A., Yeh, Joanna, Lim, Nancy, Lin, Jennifer C.Y., Taverner, Nicola, Amaya, Enrique, Papalopulu, Nancy, Smith, James C., Zorn, Aaron M., Harland, Richard M., Grammer, Timothy C.
• Format: Journal Article
• Language: English
• Published: New York Wiley Subscription Services, Inc., A Wiley Company 01.12.2002
• Subjects: Animals; Base Sequence; beta Catenin; Cytoskeletal Proteins - metabolism; development; Developmental Biology - methods; DNA, Complementary - metabolism; Ectoderm - metabolism; Endoderm - metabolism; Gene Expression Regulation, Developmental; Gene Library; Immunohistochemistry; In Situ Hybridization; Mesoderm - metabolism; Molecular Sequence Data; morpholino oligonucleotide; Oligonucleotides, Antisense - pharmacology; RNA, Messenger - metabolism; staging time table; Time Factors; Trans-Activators - metabolism; Xenopus (Silurana) tropicalis; Xenopus - embryology; Xenopus laevis; Xenopus Proteins; β‐catenin
• ISSN: 1058-8388; 1097-0177
• DOI: 10.1002/dvdy.10184

The frog Xenopus laevis has provided significant insights into developmental and cellular processes. However, X. laevis has an allotetraploid genome precluding its use in forward genetic analysis. Genetic analysis may be applicable to Xenopus (Silurana) tropicalis, which has a diploid genome and a shorter generation time. Here, we show that many tools for the study of X. laevis development can be applied to X. tropicalis. By using the developmental staging system of Nieuwkoop and Faber, we find that X. tropicalis embryos develop at similar rates to X. laevis, although they tolerate a narrower range of temperatures. We also show that many of the analytical reagents available for X. laevis can be effectively transferred to X. tropicalis. The X. laevis protocol for whole‐mount in situ hybridization to mRNA transcripts can be successfully applied to X. tropicalis without alteration. Additionally, X. laevis probes often work in X. tropicalis—alleviating the immediate need to clone the X. tropicalis orthologs before initiating developmental studies. Antibodies that react against X. laevis proteins can effectively detect the X. tropicalis protein by using established immunohistochemistry procedures. Antisense morpholino oligonucleotides (MOs) offer a new alternative to study loss of gene activity during development. We show that MOs function in X. tropicalis. Finally, X. tropicalis offers the possibility for forward genetics and genomic analysis. © 2002 Wiley‐Liss, Inc.