In this issue, Sosa et al. used bisected Xenopus laevis embryos to analyze genome-wide transcriptional regulation during twinning. The center image shows a normal tailbud whole embryo, which displays a dorsal crescent (D) and a more pigmented ventral (V) region at midblastula. In the left and right sagittal half embryos identical twins are generated. Note that the distribution of maternal pigment is asymmetric due to a 90° rotation of the Spemann-Mangold organizer center in these identical twins. Dorsal half embryos scale to form a well-patterned embryo, whereas ventral half embryos lack a dorsal axis and consist of only ventral tissues with a large coelomic cavity. The data presented represents a treasure trove of gene regulation events during early embryo regeneration. For further information, see Sosa et al., pp. 301-309.
Int. J. Dev. Biol. (2019) 63: 259-270
OPEN ACCESS
Int. J. Dev. Biol. (2019) 63: 271-280
Advanced microinjection protocol for gene manipulation using the model newt Pleurodeles waltl
Int. J. Dev. Biol. (2019) 63: 281-286
Use of soluble sperm extract to improve cloning efficiency in zebrafish
Int. J. Dev. Biol. (2019) 63: 287-293
Int. J. Dev. Biol. (2019) 63: 295-299
OPEN ACCESS
Transcriptome analysis of regeneration during Xenopus laevis experimental twinning
Int. J. Dev. Biol. (2019) 63: 301-309
Comparative analysis of p4ha1 and p4ha2 expression during Xenopus laevis development
Int. J. Dev. Biol. (2019) 63: 311-316