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      BMP4 activates the Wnt– Lin28ABlimp1–Wnt pathway to promote primordial germ cell formation via altering H3K4me2

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          ABSTRACT

          The unique developmental characteristics of chicken primordial germ cells (PGCs) enable them to be used in recovery of endangered bird species, gene editing and the generation of transgenic birds, but the limited number of PGCs greatly limits their application. Studies have shown that the formation of mammalian PGCs is induced by BMP4 signal, but the mechanism underlying chicken PGC formation has not been determined. Here, we confirmed that Wnt signaling activated via BMP4 activates transcription of Lin28A by inducing β-catenin to compete with LSD1 for binding to TCF7L2, causing LSD1 to dissociate from the Lin28A promoter and enhancing H3K4me2 methylation in this region. Lin28A promotes PGC formation by inhibiting gga-let7a-3p maturation to initiate Blimp1 expression. Interestingly, expression of Blimp1 helped sustain Wnt5A expression by preventing LSD1 binding to the Wnt5A promoter. We thus elucidated a positive feedback pathway involving Wnt– Lin28ABlimp1–Wnt that ensures PGC formation. In summary, our data provide new insight into the development of PGCs in chickens .

          Abstract

          Summary: We describe a Wnt– Lin28ABlimp1–Wnt positive feedback regulation system during the formation of primordial germ cells, which is regulated by upstream BMP4 signals and H3K4me2.

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          Most cited references55

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          Identification of c-MYC as a target of the APC pathway.

          The adenomatous polyposis coli gene (APC) is a tumor suppressor gene that is inactivated in most colorectal cancers. Mutations of APC cause aberrant accumulation of beta-catenin, which then binds T cell factor-4 (Tcf-4), causing increased transcriptional activation of unknown genes. Here, the c-MYC oncogene is identified as a target gene in this signaling pathway. Expression of c-MYC was shown to be repressed by wild-type APC and activated by beta-catenin, and these effects were mediated through Tcf-4 binding sites in the c-MYC promoter. These results provide a molecular framework for understanding the previously enigmatic overexpression of c-MYC in colorectal cancers.
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            Bmp4 is required for the generation of primordial germ cells in the mouse embryo.

            In many organisms the allocation of primordial germ cells (PGCs) is determined by the inheritance of maternal factors deposited in the egg. However, in mammals, inductive cell interactions are required around gastrulation to establish the germ line. Here, we show that Bmp4 homozygous null embryos contain no PGCs. They also lack an allantois, an extraembryonic mesodermal tissue derived, like the PGCs, from precursors in the proximal epiblast. Heterozygotes have fewer PGCs than normal, due to a reduction in the size of the founding population and not to an effect on its subsequent expansion. Analysis of beta-galactosidase activity in Bmp4(lacZneo) embryos reveals that prior to gastrulation, Bmp4 is expressed in the extraembryonic ectoderm. Later, Bmp4 is expressed in the extraembryonic mesoderm, but not in PGCs. Chimera analysis indicates that it is the Bmp4 expression in the extraembryonic ectoderm that regulates the formation of allantois and primordial germ cell precursors, and the size of the founding population of PGCs. The initiation of the germ line in the mouse therefore depends on a secreted signal from the previously segregated, extraembryonic, trophectoderm lineage.
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              A molecular programme for the specification of germ cell fate in mice.

              Germ cell fate in mice is induced in proximal epiblast cells by the extra-embryonic ectoderm, and is not acquired through the inheritance of any preformed germ plasm. To determine precisely how germ cells are specified, we performed a genetic screen between single nascent germ cells and their somatic neighbours that share common ancestry. Here we show that fragilis, an interferon-inducible transmembrane protein, marks the onset of germ cell competence, and we propose that through homotypic association, it demarcates germ cells from somatic neighbours. Using single-cell gene expression profiles, we also show that only those cells with the highest expression of fragilis subsequently express stella, a gene that we detected exclusively in lineage-restricted germ cells. The stella positive nascent germ cells exhibit repression of homeobox genes, which may explain their escape from a somatic cell fate and the retention of pluripotency.
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                Author and article information

                Journal
                J Cell Sci
                J Cell Sci
                JCS
                joces
                Journal of Cell Science
                The Company of Biologists Ltd
                0021-9533
                1477-9137
                1 February 2021
                1 February 2021
                1 February 2021
                : 134
                : 3
                : jcs249375
                Affiliations
                [1 ]Key Laboratory of Animal Breeding Reproduction and Molecular Design for Jiangsu Province, College of Animal Science and Technology, Yangzhou University , Yangzhou, Jiangsu 225009, China
                [2 ]Joint International Research Laboratory of Agriculture and Agri-Product Safety, The Ministry of Education of China, Yangzhou University , Yangzhou, Jiangsu 225009, China
                Author notes
                [*]

                These authors contributed equally to this work

                []Author for correspondence ( yubcli@ 123456yzu.edu.cn )

                Handling Editor: John Heath

                Author information
                http://orcid.org/0000-0003-0209-0479
                Article
                JCS249375
                10.1242/jcs.249375
                7875490
                33443086
                d4a34c1f-c79c-4807-a650-c36afb780101
                © 2021. Published by The Company of Biologists Ltd

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 26 May 2020
                : 11 December 2020
                Funding
                Funded by: Jiangsu Science and Technology Project;
                Award ID: BK20180918
                Funded by: Natural Science Research Project of Jiangsu Higher Education Institutions;
                Award ID: 18KJB230008
                Funded by: Jiangsu Provincial Key Research and Development Program;
                Award ID: 2017YFE0108000
                Funded by: National Natural Science Foundation of China, http://dx.doi.org/10.13039/501100001809;
                Award ID: 31872341
                Funded by: Yangzhou University, http://dx.doi.org/10.13039/501100007062;
                Award ID: 11117
                Categories
                135
                126
                Research Article

                Cell biology
                chicken,primordial germ cells,h3k4me2,lin28a,wnt signaling
                Cell biology
                chicken, primordial germ cells, h3k4me2, lin28a, wnt signaling

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