| Autor: |
Murdaugh LB; Bowles Center for Alcohol Studies, University of North Carolina, Chapel Hill, North Carolina, United States of America., Mendoza-Romero HN; Bowles Center for Alcohol Studies, University of North Carolina, Chapel Hill, North Carolina, United States of America., Fish EW; Bowles Center for Alcohol Studies, University of North Carolina, Chapel Hill, North Carolina, United States of America., Parnell SE; Bowles Center for Alcohol Studies, University of North Carolina, Chapel Hill, North Carolina, United States of America.; Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, North Carolina, United States of America.; Carolina Institute for Developmental Disabilities, University of North Carolina, Chapel Hill, North Carolina, United States of America. |
| Abstrakt: |
In many experiments using fetal mice, it is necessary to determine the sex of the individual fetus. However, other than genotyping for sex-specific genes, there is no convenient, reliable method of sexing mice between gestational day (GD) 16.5 and GD 18.0. We designed a rapid, relatively simple visual method to determine the sex of mouse fetuses in the GD 16.5-GD 18.0 range that can be performed as part of a routine morphological assessment. By examining the genitalia for the presence or absence of key features, raters with minimal experience with the method were able to correctly identify the sex of embryos with 99% accuracy, while raters with no experience were 95% accurate. The critical genital features include: the presence or absence of urethral seam or proximal urethral meatus; the shape of the genitalia, and the presence or absence of an area related to the urethral plate. By comparing these morphological features of the external genitalia, we show a simple, accurate, and fast way to determine the sex of late stage mouse fetuses. Integrating this method into regular morphological assessments will facilitate the determination of sex differences in fetuses between GD 16.5 and GD 18.0. |
