An illustrated anatomical ontology of the developing mouse lower urogenital tract

Author:

Georgas Kylie M.1,Armstrong Jane2,Keast Janet R.3,Larkins Christine E.4,McHugh Kirk M.5,Southard-Smith E. Michelle6,Cohn Martin J.478,Batourina Ekatherina9,Dan Hanbin9,Schneider Kerry9,Buehler Dennis P.6,Wiese Carrie B.6,Brennan Jane2,Davies Jamie A.2,Harding Simon D.10,Baldock Richard A.10,Little Melissa H.1,Vezina Chad M.11,Mendelsohn Cathy9

Affiliation:

1. Institute for Molecular Bioscience, The University of Queensland, St Lucia, Queensland 4072, Australia

2. Center for Integrative Physiology, University of Edinburgh, Edinburgh EH8 9XD, UK

3. Department of Anatomy and Neuroscience, University of Melbourne, Parkville, Victoria 3010, Australia

4. Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL 32610, USA

5. Centre for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital and Division of Anatomy, The Ohio State University, Columbus, OH 43205/10, USA

6. Division of Genetic Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232, USA

7. Department of Biology, Genetics Institute, University of Florida, Gainesville, FL 32610, USA

8. Howard Hughes Medical Institute, University of Florida, Gainesville, FL 32610, USA

9. Columbia University, Department of Urology, New York, NY 10032, USA

10. MRC Human Genetics Unit, MRC IGMM, Western General Hospital, Edinburgh EH4 2XU, UK

11. University of Wisconsin-Madison, School of Veterinary Medicine, Madison, WI 53706, USA

Abstract

Malformation of the urogenital tract represents a considerable paediatric burden, with many defects affecting the lower urinary tract (LUT), genital tubercle and associated structures. Understanding the molecular basis of such defects frequently draws on murine models. However, human anatomical terms do not always superimpose on the mouse, and the lack of accurate and standardised nomenclature is hampering the utility of such animal models. We previously developed an anatomical ontology for the murine urogenital system. Here, we present a comprehensive update of this ontology pertaining to mouse LUT, genital tubercle and associated reproductive structures (E10.5 to adult). Ontology changes were based on recently published insights into the cellular and gross anatomy of these structures, and on new analyses of epithelial cell types present in the pelvic urethra and regions of the bladder. Ontology changes include new structures, tissue layers and cell types within the LUT, external genitalia and lower reproductive structures. Representative illustrations, detailed text descriptions and molecular markers that selectively label muscle, nerves/ganglia and epithelia of the lower urogenital system are also presented. The revised ontology will be an important tool for researchers studying urogenital development/malformation in mouse models and will improve our capacity to appropriately interpret these with respect to the human situation.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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