The DOI matches its Crossref record.
Mechanisms of reduced fertility in Hoxa-10 mutant mice: uterine homeosis and loss of maternal Hoxa-10 expression
Abstract
The establishment of a receptive uterine environment is critical for embryonic survival and implantation. One gene that is expressed in the uterus during the peri-implantation period in mice and is required for female fertility is the homeobox gene Hoxa-10. Here we characterize the periimplantation defects in Hoxa-10 mutant females and investigate functions of Hoxa-10 in the uterine anlage during morphogenesis and in the adult uterus during pregnancy. Examination of pregnancy in Hoxa-10 mutant females has revealed failure of implantation as well as resorption of embryos in the early postimplantation period. Morphologic analysis of the mutant uterus has demonstrated homeotic transformation of the proximal 25% into oviduct. Histology and molecular markers confirm this anterior transformation. Furthermore, in situ hybridization shows that this region coincides with the anterior limit of embryonic Hoxa-10 expression in the urogenital ducts and a parallel transformation is observed in Hoxa-10 mutant males at the junction of the epididymis and ductus deferens. Female fertility could be compromised by either the homeotic transformation or the absence of Hoxa-10 function in the adult during pregnancy. To distinguish between these two potential mechanisms of infertility, wildtype blastocysts were transferred into mutant uteri distal to the transformed region on day 2.5 of pseudopregnancy. This procedure did not rescue the phenotype, suggesting that adult uterine expression of Hoxa-10 is required during pregnancy. Moreover, when implantation was experimentally delayed, homozygous uteri were able to support survival of blastocysts comparable to wild-type controls, indicating that the requirement for Hoxa-10 is intrinsic to implantation. While expression of LIF and HB-EGF appears unaffected in the mutant uteri, a decrease is observed in the intensity and number of blue dye reactions, an indicator of increased vascular permeability in response to implantation. In addition, mutant uteri exhibited decreased decidualization in response to artificial stimuli. These results show that Hoxa-10 is required during morphogenesis for proper patterning of the reproductive tract and in the adult uterus for peri-implantation events.
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
Cited by
Multiple Female Reproductive Failures in Cyclooxygenase 2–Deficient Mice
Lim, H., Paria, B. C., Das, S. K., Dinchuk, J. E., Langenbach, R., Trzaskos, J. M., & Dey, S. K. (1997) · Cell · doi:10.1016/s0092-8674(00)80402-x · Cited by 1,430
Self-citationMechanisms of implantation: strategies for successful pregnancy
Cha, J., Sun, X., & Dey, S. K. (2012) · Nature Medicine · doi:10.1038/nm.3012 · Cited by 1,357
Self-citationRoadmap to embryo implantation: clues from mouse models
Wang, H., & Dey, S. K. (2006) · Nature Reviews Genetics · doi:10.1038/nrg1808 · Cited by 1,298
Self-citationTrophoblast differentiation during embryo implantation and formation of the maternal-fetal interface
Red-Horse, K., Zhou, Y., Genbacev, O., Prakobphol, A., Foulk, R., McMaster, M., & Fisher, S. J. (2004) · Journal of Clinical Investigation · doi:10.1172/jci200422991 · Cited by 786
Endocrine regulation of menstruation
Jabbour, H. N., Kelly, R. W., Fraser, H. M., & Critchley, H. O. D. (2006) · Endocrine Reviews · doi:10.1210/er.2004-0021 · Cited by 588
Physiological and molecular determinants of embryo implantation
Zhang, S., Lin, H., Kong, S., Wang, S., Wang, H., Wang, H., & Armant, D. R. (2013) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2012.12.011 · Cited by 587
Endometrial Decidualization: Of Mice and Men
Ramathal, C., Bagchi, I., Taylor, R., & Bagchi, M. (2010) · Seminars in Reproductive Medicine · doi:10.1055/s-0029-1242989 · Cited by 517
Miller, C., & Sassoon, D. A. (1998) · Development · doi:10.1242/dev.125.16.3201 · Cited by 400
Warot, X., Fromental-Ramain, C., Fraulob, V., Chambon, P., & Dollé, P. (1997) · Development · doi:10.1242/dev.124.23.4781 · Cited by 358
Paria, B. C., Ma, W.-G., Tan, J., Raja, S., Das, S. K., Dey, S. K., & Hogan, B. L. M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.3.1047 · Cited by 352
Self-citationEndocrine Regulation of HOX Genes
Daftary, G. S., & Taylor, H. S. (2006) · Endocrine Reviews · doi:10.1210/er.2005-0018 · Cited by 344
Defective implantation and placentation: laying the blueprint for pregnancy complications
Norwitz, E. R. (2006) · Reproductive BioMedicine Online · doi:10.1016/s1472-6483(10)60649-9 · Cited by 332
Lim, H. J., Ma, L., Ma, W., Maas, R. L., & Dey, S. K. (1999) · Molecular Endocrinology · doi:10.1210/me.13.6.1005 · Cited by 326
Self-citationHomeobox Genes in Embryogenesis and Pathogenesis
Mark, M., Rijli, F. M., & Chambon, P. (1997) · Pediatric Research · doi:10.1203/00006450-199710000-00001 · Cited by 318
The Role of Growth Factors and Cytokines during Implantation: Endocrine and Paracrine Interactions
Guzeloglu-Kayisli, O., Kayisli, U., & Taylor, H. (2009) · Seminars in Reproductive Medicine · doi:10.1055/s-0028-1108011 · Cited by 314
Hypospadias and endocrine disruption: is there a connection?
Baskin, L. S., Himes, K., & Colborn, T. (2001) · Environmental Health Perspectives · doi:10.1289/ehp.011091175 · Cited by 281
Tan, J., Paria, B. C., Dey, S. K., & Das, S. K. (1999) · Endocrinology · doi:10.1210/endo.140.11.7148 · Cited by 278
Self-citationBlock, K., Kardana, A., Igarashi, P., & Taylor, H. S. (2000) · The FASEB Journal · doi:10.1096/fasebj.14.9.1101 · Cited by 257
Rackow, B. W., & Taylor, H. S. (2010) · Fertility and Sterility · doi:10.1016/j.fertnstert.2008.03.029 · Cited by 239
Altered expression of HOXA10 in endometriosis: potential role in decidualization
Kim, J. J., Taylor, H. S., Lu, Z., Ladhani, O., Hastings, J. M., Jackson, K. S., Wu, Y., Guo, S. W., & Fazleabas, A. T. (2007) · MHR: Basic science of reproductive medicine · doi:10.1093/molehr/gam005 · Cited by 228
Lee, B., Du, H., & Taylor, H. S. (2009) · Biology of Reproduction · doi:10.1095/biolreprod.108.070391 · Cited by 204
Regulation of HOXA-10 and its expression in normal and abnormal endometrium
Gui, Y., Zhang, J., Yuan, L., & Lessey, B. A. (1999) · MHR: Basic science of reproductive medicine · doi:10.1093/molehr/5.9.866 · Cited by 139
MicroRNA 135 regulates HOXA10 expression in endometriosis
Petracco, R., Grechukhina, O., Popkhadze, S., Massasa, E., Zhou, Y., & Taylor, H. S. (2011) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2011-1231 · Cited by 138
HOXA9 promotes ovarian cancer growth by stimulating cancer-associated fibroblasts
Ko, S. Y., Barengo, N., Ladanyi, A., Lee, J.-S., Marini, F., Lengyel, E., & Naora, H. (2012) · Journal of Clinical Investigation · doi:10.1172/jci62229 · Cited by 132
Cakmak, H., & Taylor, H. (2010) · Seminars in Reproductive Medicine · doi:10.1055/s-0029-1242996 · Cited by 105
FKBP4 is regulated by HOXA10 during decidualization and in endometriosis
Yang, H., Zhou, Y., Edelshain, B., Schatz, F., Lockwood, C. J., & Taylor, H. S. (2012) · Reproduction · doi:10.1530/rep-11-0438 · Cited by 63
Metadata
- Authors
- Benson, G. V., Lim, H., Paria, B. C., Satokata, I., Dey, S. K., & Maas, R. L.
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 1996-09-01
- Volume
- 122
- Issue
- 9
- Pages
- 2687-2696
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W2145290390
- Cited by
- 501
- References
- 0
- FWCI
- 4.25
- 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.