Mohawk (Mkx) is a member of the Three Amino acid Loop Extension superclass of atypical homeobox genes that is expressed in developing tendons. To investigate the in vivo functions of Mkx, we generated Mkx −/− mice. These mice had hypoplastic tendons throughout the body. Despite the reduction in tendon mass, the cell number in tail tendon fiber bundles was similar between wild-type and Mkx −/− mice. We also observed small collagen fibril diameters and a down-regulation of type I collagen in Mkx −/− tendons. These data indicate that Mkx plays a critical role in tendon differentiation by regulating type I collagen production in tendon cells.T endons are dense, fibrous connective tissues that connect muscle to bone, transmitting the forces that allow for body movement (1). Tendon damage from overuse or degeneration due to aging is a common clinical problem because damaged tendon tissue heals very slowly and rarely recovers completely (2). The establishment of new therapies, such as regenerative medicine, for injured tendons has been delayed by a limited understanding of tendon biology (1, 3).Tendons are composed primarily of collagen fibrils that cross-link to each other to form fibers (4). A small number of tendon cells reside between parallel chains of these fibrils and synthesize the specific ECM that contains collagens and proteoglycans (4, 5). The elasticity of tendons is provided by the large amount of collagen, predominantly type I collagen and small amounts of other collagens, including types III, IV, V, and VI (4, 6-9). The proteoglycans found in tendons, including decorin, fibromodulin, biglycan, and lumican, act to lubricate and organize collagen fiber bundles (4, 5). Targeted disruption of these proteoglycans in mice leads to abnormal collagen fibrils in tendons (3, 10-13). Tendon disruptions have also been described in patients with defects in collagen production, such as Ehlers-Danlos Syndrome, in which the type I collagen gene is mutated (14). These studies indicate that the ability of tendon cells to produce ECM is important for tendon formation.Recently, it was reported that Scleraxis (Scx), a basic helix-loophelix (bHLH) transcription factor expressed in the tendon progenitors and cells of all tendon tissues (15, 16), is essential for tendon differentiation. Scx knockout mice show severe disruption of force-transmitting tendons, although ligaments, which are tissues connecting bone to bone that closely resemble tendons in their components, and short-range anchoring tendons are not affected (17). It was also reported that Scx positively regulates the expression of type I collagen, a main ECM component of tendons (18). However, the type I collagen does not completely disappear from the tendons of Scx knockout mice (17), suggesting the presence of other regulatory factors for type I collagen. The tendon differentiation mechanisms remain largely unknown, with Scx being the only known transcription factor regulating tendon differentiation.Mohawk (Mkx; also known as Irxl1) is the sole member of a newly c...

SUMMARY We created a whole-mount in situ hybridization (WISH) database, termed EMBRYS, containing expression data of 1520 transcription factors and cofactors expressed in E9.5, E10.5, and E11.5 mouse embryos—a highly dynamic stage of skeletal myogenesis. This approach implicated 43 genes in regulation of embryonic myogenesis, including a transcriptional repressor, the zinc-finger protein RP58 (also known as Zfp238). Knockout and knockdown approaches confirmed an essential role for RP58 in skeletal myogenesis. Cell-based high-throughput transfection screening revealed that RP58 is a direct MyoD target. Microarray analysis identified two inhibitors of skeletal myogenesis, Id2 and Id3, as targets for RP58-mediated repression. Consistently, MyoD-dependent activation of the myogenic program is impaired in RP58 null fibroblasts and downregulation of Id2 and Id3 rescues MyoD’s ability to promote myogenesis in these cells. Our combined, multi-system approach reveals a MyoD-activated regulatory loop relying on RP58-mediated repression of muscle regulatory factor (MRF) inhibitors.

The transcription factor, Sry-related High Mobility Group (HMG) box containing gene 9 (Sox9), plays a critical role in cartilage development by initiating chondrogenesis and preventing the subsequent maturation process called chondrocyte hypertrophy. This suppression mechanism by Sox9 on late-stage chondrogenesis partially results from the inhibition of Runt-related transcription factor 2 (Runx2), the main activator of hypertrophic chondrocyte differentiation. However, the precise mechanism by which Sox9 regulates late chondrogenesis is poorly understood.In the present study, the transcriptional repressor vertebrate homolog of Drosophila bagpipe (Bapx1) was found to be a direct target of Sox9 for repression of Runx2 expression in chondrocytes. We identified a critical Sox9 responsive region in the Bapx1 promoter via a luciferase reporter assay. Analysis by chromatin immunoprecipitation and electrophoretic mobility shift assays indicated that Sox9 physically bound to this region of the Bapx1 promoter. Consistent with the notion that Bapx1 and Sox9 act as negative regulators of chondrocyte hypertrophy by regulating Runx2 expression, transient knockdown of Sox9 or Bapx1 expression by shRNA in chondrocytes increased Runx2 expression, as well as expression of the late chondrogenesis marker, Col10a1. Furthermore, while over-expression of Sox9 decreased Runx2 and Col10a1 expressions, simultaneous transient knockdown of Bapx1 diminished that Sox9 over-expressing effect.Our findings reveal that the molecular pathway modulated by Bapx1 links two major regulators in chondrogenesis, Sox9 and Runx2, to coordinate skeletal formation.

The Caenorhabditis elegans heterochronic gene lin-28 regulates developmental timing in the nematode trunk. We report the dynamic expression patterns of Lin-28 homologues in mouse and chick embryos. Whole mount in situ hybridization revealed specific and intriguing expression patterns of Lin-28 in the developing mouse and chick limb bud. Mouse Lin-28 expression was detected in both the fore-limb and hindlimb at E9.5, but disappeared from the forelimb at E10.5, and finally from the forelimb and hindlimb at E11.5. Chicken Lin-28, which was first detected in the limb primordium at stage 15/16, was also downregulated as the stage proceeded. The amino acid sequences of mouse and chicken Lin-28 genes are highly conserved and the similar expression patterns of Lin-28 during limb development in mouse and chicken suggest that this heterochronic gene is also conserved during vertebrate limb development. KeywordsHeterochronic gene; Whole mount in situ hybridization; Mouse; Chick; Limb bud; Lin-28; MicroRNAs; Developmental timing; Dynamic expression; Embryo Results and discussionEmbryonic development is tightly regulated by spatio-temporal gene expression; however, systems regulating developmental timing are largely unknown. A series of mutagenesis studies using the nematode Caenorhabditis elegans as a model have identified a cluster of genes, the so-called "heterochronic genes," which is expressed at the specific period of time during embryogenesis and play a critical role in determining the relative timing of developmental events (Ambros and Horvitz, 1984;Lee et al., 1993). Among these heterochronic genes, * Corresponding author. Address: Department of Systems Biomedicine, National Research Institute for Child Health and Development, 2-10-1 Okura, Setagaya, Tokyo, Japan. Tel/fax: +81 3 3417 2498., E-mail address: asahara@nch.go.jp (H. Asahara). Publisher's Disclaimer: This article was published in an Elsevier journal. The attached copy is furnished to the author for non-commercial research and education use, including for instruction at the author's institution, sharing with colleagues and providing to institution administration. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. To further examine the spatio-temporal expression patterns of Lin-28 in developing embryos, we performed whole mount in situ hybridization using mouse and chicken embryos at different developmental stages.Although Lin-28 was ubiquitously expressed throughout the mouse embryo at E9.5 (Fig. 1a, a′), strong expression was observed in the most distal mesenchyme adjacent to the apical ectodermal ridge (AER) of both forelimb and hindlimb buds (Fig. 1b, b′, white arrow). Interestingly, at E10.5, the expression of Lin-28 in forelimb almost disappeared, and expression was restricted to the hindlimb and more caudal trunk at the hindlimb level ( Fig. 1c-e). In a ...

The body plan along the anteroposterior axis and regional identities are specified by the spatiotemporal expression of Hox genes. Multistep controls are required for their unique expression patterns; however, the molecular mechanisms behind the tight control of Hox genes are not fully understood. In this study, we demonstrated that the Lin28a/let-7 pathway is critical for axial elongation. Lin28a–/– mice exhibited axial shortening with mild skeletal transformations of vertebrae, which were consistent with results in mice with tail bud-specific mutants of Lin28a. The accumulation of let-7 in Lin28a–/– mice resulted in the reduction of PRC1 occupancy at the Hox cluster loci by targeting Cbx2. Consistently, Lin28a loss in embryonic stem-like cells led to aberrant induction of posterior Hox genes, which was rescued by the knockdown of let-7. These results suggest that the Lin28/let-7 pathway is involved in the modulation of the ‘Hox code’ via Polycomb regulation during axial patterning.

44The body plan along the anteroposterior axis and regional identities are specified by the 45 spatiotemporal expression of Hox genes. Multistep controls are required for their unique 46 expression patterns; however, the molecular mechanisms behind the tight control of 47 Hox genes are not fully understood. In this study, we demonstrated that the Lin28a/let-7 48 reciprocal regulatory pathway is critical for vertebral specification. Lin28a -/mice 49 exhibited homeotic transformations of vertebrae which were caused by the global 50 dysregulation of posterior Hox genes. The accumulation of let-7-family microRNAs in 51 Lin28a -/mice resulted in the reduction of PRC1 occupancy at the Hox cluster loci by 52 targeting Cbx2. Consistently, Lin28a loss in embryonic stem-like cells led to aberrant 53 induction of posterior Hox genes, which was rescued by the knockdown of let-7-family 54 microRNAs. These results suggest that Lin28/let-7 pathway is possibly involved in the 55 modulation of the "Hox code" via Polycomb regulation during axial patterning in 56 vertebrates. 57 58 59 60 61 62 63 64 65 expression. However, the molecular mechanisms underlying the termination of PcG 88 gene expression remain largely unclear. 89Previously, we generated a whole-mount in situ hybridization database called 90 "EMBRYS" that covers ~1,600 transcription factors and RNA-binding factors using mice 91 at embryonic day (E)9.5, E10.5, and E11.5 (Yokoyama et al., 2009). Among these data, 92we were particularly interested in dynamic expressional changes of Lin28a during 93 embryogenesis: at E9.5, Lin28a is expressed ubiquitously, whereas its expression 94 gradually diminishes from head to tail at E10.5 and E11.5 (Yokoyama et al., 2008, 95

No abstract