# DCAF13 is essential for mouse uterine function and fertility

**Authors:** Qianhui Zhou, Xiaohui Li, Ningjing Wang, Liang Zhang, Enhui Jiang, Kaixuan Wang, Xingyu Yan, Cong Zhang

PMC · DOI: 10.1038/s41420-025-02583-w · Cell Death Discovery · 2025-08-01

## TL;DR

This study shows that DCAF13 is crucial for mouse uterine development and fertility, as its absence leads to infertility due to disrupted hormone signaling and cell proliferation.

## Contribution

The study reveals a novel role for DCAF13 in regulating uterine function and fertility through hormone receptor expression and epigenetic regulation.

## Key findings

- DCAF13 knockout mice show reduced uterine size and infertility due to impaired embryo implantation.
- DCAF13 regulates estrogen and progesterone receptor expression and methylation-related genes like SUV39H2.
- Loss of DCAF13 increases H3K9me3 levels, hindering endometrial cell proliferation.

## Abstract

The incidence of female infertility is a growing worldwide concern and a leading cause of population decline. Therefore, understanding the pathogenesis of infertility is of utmost importance. DDB1 and CUL4 Associated Factor 13 (DCAF13) is a significant component of the CRL4 E3 ubiquitin ligase complex responsible for recognizing substrates and degrading them after polyubiquitylation. DCAF13 has been implicated in oocyte and embryo development, but its role in the uterus remains elusive. To investigate its function, we generated Dcaf13 conditional knockout (cKO) mice and discovered that the uteri of cKO mice became smaller and thinner as they mature, and the embryos were unable to implant, leading to infertility. Mechanistically, we detected aberrant expression of estrogen and progesterone receptors, along with dysregulation of estrogen- and progesterone-responsive genes in the endometrium. This led to insufficient proliferation of endometrial cells in mice. RNAseq analysis revealed an overall increase in transcription of methylation-related genes, including SUV39H2, leading to higher H3K9me3 levels and consequently hindered cell proliferation in the uterus. Furthermore, DCAF13 knockdown resulted in elevated intracellular H3K9me3 levels. In conclusion, these findings suggest that DCAF13 is essential for maintaining the structure of the uterus and fertility. This study potentially contributes to the development of new strategies aimed at improving female reproductive health.

## Linked entities

- **Genes:** DCAF13 (DDB1 and CUL4 associated factor 13) [NCBI Gene 25879], SUV39H2 (SUV39H2 histone lysine methyltransferase) [NCBI Gene 79723]
- **Proteins:** DCAF13 (DDB1 and CUL4 associated factor 13)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Foxa2 (forkhead box A2) [NCBI Gene 15376] {aka HNF3-beta, HNF3beta, Hnf-3b, Hnf3b, Tcf-3b, Tcf3b}, Egf (epidermal growth factor) [NCBI Gene 13645], Wnt7a (wingless-type MMTV integration site family, member 7A) [NCBI Gene 22421] {aka Wnt-7a, px, tw}, Dcaf13 (DDB1 and CUL4 associated factor 13) [NCBI Gene 223499] {aka Gm83, Wdsof1}, Pten (phosphatase and tensin homolog) [NCBI Gene 19211] {aka 2310035O07Rik, A130070J02Rik, B430203M17Rik, MMAC1, PTENbeta, TEP1}, Muc1 (mucin 1, transmembrane) [NCBI Gene 17829] {aka CD227, EMA, Muc-1}, Spink1 (serine peptidase inhibitor, Kazal type 1) [NCBI Gene 20730] {aka Spink3, p12}, Ihh (Indian hedgehog) [NCBI Gene 16147] {aka HHG-2}, SUV39H1 (SUV39H1 histone lysine methyltransferase) [NCBI Gene 6839] {aka H3-K9-HMTase 1, KMT1A, MG44, SUV39H}, Cdh1 (cadherin 1) [NCBI Gene 12550] {aka ARC-1, E-cad, Ecad, L-CAM, UVO, Um}, Ltf (lactotransferrin) [NCBI Gene 17002] {aka Csp82, Lf, MMS10R, Ms10r}, Areg (amphiregulin) [NCBI Gene 11839] {aka AR, Mcub, Sdgf}, Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345] {aka D630048A14Rik, Ki-67, Ki67}, Clca1 (chloride channel accessory 1) [NCBI Gene 23844] {aka Clca2, Clca3, gob-5, gob5}, Krt18 (keratin 18) [NCBI Gene 16668] {aka CK18, K18, Krt1-18}, Dcaf11 (DDB1 and CUL4 associated factor 11) [NCBI Gene 28199] {aka 0710008A13Rik, D14Ucla1, Dacf11, GLO14, Wdr23}, Lif (leukemia inhibitory factor) [NCBI Gene 16878], H2ax (H2A.X variant histone) [NCBI Gene 15270] {aka H2A.X, H2afx, Hist5-2ax, gammaH2ax}, Hand2 (heart and neural crest derivatives expressed 2) [NCBI Gene 15111] {aka Ehand2, Hed, Th2, Thing2, bHLHa26, dHAND}, Esr1 (estrogen receptor 1 (alpha)) [NCBI Gene 13982] {aka ER, ER-alpha, ERa, ERalpha, ESR, Estr}, Suv39h2 (suppressor of variegation 3-9 2) [NCBI Gene 64707] {aka 4930507K23Rik, D030054H19Rik, D2Ertd544e, KMT1B}, Lrp2 (low density lipoprotein receptor-related protein 2) [NCBI Gene 14725] {aka D230004K18Rik, Gp330, Megalin, b2b1625.2Clo}, Wfdc3 (WAP four-disulfide core domain 3) [NCBI Gene 71856] {aka 1700015L13Rik, 1700127F16Rik}, Suv39h1 (suppressor of variegation 3-9 1) [NCBI Gene 20937] {aka DXHXS7466e, H3-K9-HMTase 1, KMT1A, mIS6}, Nr2f2 (nuclear receptor subfamily 2, group F, member 2) [NCBI Gene 11819] {aka 2700033K02Rik, 9430015G03Rik, ARP-1, Aporp1, COUP-TF2, COUP-TFII}, Lcn2 (lipocalin 2) [NCBI Gene 16819] {aka 24p3, NRL, Sip24}, Casp3 (caspase 3) [NCBI Gene 12367] {aka A830040C14Rik, AC-3, CASP-3, CC3, CPP-32, CPP32}, Actb (actin, beta) [NCBI Gene 11461] {aka Actx, E430023M04Rik, beta-actin}, Pgr (progesterone receptor) [NCBI Gene 18667] {aka 9930019P03Rik, NR3C3, PR, PR-A, PR-B}, Ddb1 (damage specific DNA binding protein 1) [NCBI Gene 13194] {aka 127kDa, p127-Ddb1}, Ung (uracil DNA glycosylase) [NCBI Gene 22256] {aka UNG1, UNG2}, DCAF13 (DDB1 and CUL4 associated factor 13) [NCBI Gene 25879] {aka GM83, HSPC064, Sof1, WDSOF1}, Pik3r1 (phosphoinositide-3-kinase regulatory subunit 1) [NCBI Gene 18708] {aka PI3K, p50alpha, p55alpha, p85alpha}, Wnt4 (wingless-type MMTV integration site family, member 4) [NCBI Gene 22417] {aka Wnt-4}, Mul1 (mitochondrial ubiquitin ligase activator of NFKB 1) [NCBI Gene 68350] {aka 0610009K11Rik, Gide, Tnrip-1}, SUV39H2 (SUV39H2 histone lysine methyltransferase) [NCBI Gene 79723] {aka KMT1B}
- **Diseases:** cancers (MESH:D009369), infertility (MESH:D007246), bleeding (MESH:D006470), female infertility (MESH:D007247), endometrial thinning (MESH:D013851), cervical cancer (MESH:D002583)
- **Chemicals:** CO2 (MESH:D002245), water (MESH:D014867), HE (MESH:D006371), alcohol (MESH:D000438), SDS (MESH:D012967), eosin (MESH:D004801), hyaluronic acid (MESH:D006820), paraformaldehyde (MESH:C003043), hydrogen peroxide (MESH:D006861), DMEM/F12 (-), hydrochloric acid (MESH:D006851), citric acid (MESH:D019343), Progesterone (MESH:D011374), trypan blue (MESH:D014343), TRIzol (MESH:C411644), hematoxylin (MESH:D006416), paraffin (MESH:D010232), ethanol (MESH:D000431), xylene (MESH:D014992), poly-A (MESH:D011061), polyvinylidene fluoride (MESH:C024865)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU), Hela — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030), HeLa — Homo sapiens (Human), Human papillomavirus-related cervical squamous cell carcinoma, Cancer cell line (CVCL_T292)

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Source: https://tomesphere.com/paper/PMC12316921