03-P068 Mechanoregulation of patterning genes during mouse skeletal development: Growth and differentiation in the absence of muscle contractions

نویسندگان

  • Celine Bourdon
  • Patrick Prendergast
  • Paula Murphy
  • Shahragim Tajbakhsh
چکیده

islands in the extraembryonic yolk sac. This observation has led to the hypothesis that both cell types originate from a common precursor known as the hemangioblast. This hypothesis has been supported mainly by the co-expression of several genes in both cell types and by in vitro differentiation studies. However, recent studies indicate that primitive blood cells originate from an intermediate population of hemogenic endothelial cells. Chick Cerberus gene (cCer) codes for a secreted factor expressed in the anterior mesendoderm that gives rise to blood islands, among other tissues. During the study of cCer transcriptional regulation in chick embryos, we isolated a short cis-regulatory region that is able to drive reporter gene expression specifically in blood island precursor cells or hemangioblasts. We have been using this hemangioblast-specific reporter construct (Hb-eGFP) to characterise the gene expression profile of the chick hemangioblast and to track the origin and fate of hemangioblasts in living embryos. Here, we will present data on the gene expression profile of the early chick hemangioblast as well as on the dynamics of blood island morphogenesis and differentiation.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Genome-wide Association Study to Identify Genes and Biological Pathways Associated with Type Traits in Cattle using Pathway Analysis

Extended Abstract Introduction and Objective: Type traits describing the skeletal characteristics of an animal are moderately to strongly genetically correlate with other economically important traits in cattle including fertility, longevity and carcass traits. The present study aimed to conduct a genome wide association studies (GWAS) based on gene-set enrichment analysis for identifying the ...

متن کامل

Ursolic Acid Improve Skeletal Muscle Hypertrophy by Increasing of PAX7, Myod and Myogenin Expression and Satellite Cells Proliferation in Native Broiler Chickens

Ursolic acid (UA) is known as a naturally occurring triterpene pentacyclic compound in some medicinal herbs including savory that affects the skeletal muscle. In the current study, the effect of UA was evaluated on C2C12 cells and satellite cells (SCs) isolated from native broiler chicks. First in the in vitro experiment, the C2C12 cell line obtained from the Stem Cell Technology Research Cente...

متن کامل

Effect of lysophosphatidic acid on the follicular development and the ‎expression of lysophosphatidic acid receptor genes during in vitro culture of ‎mouse ovary

Lysophosphatidic acid (LPA) known as a serum-derived growth factor, is involved in several cell physiological functions in the female reproductive system including: oocyte maturation, in vitro fertilization and embryo implantation by its transmembrane G protein-coupled receptors. The aim of the present study was to examine the effect of LPA on in vitro follicular development o...

متن کامل

Effects of in ovo Injection of Zinc Acetate on some Gene Expression Associated with Embryonic Growth and Development, and with Growth and Carcass Characteristics of the Resultant Chicks

This study was conducted in two steps to determine the effects of in ovo injection of zinc acetate (ZAC) on some gene expression associated with embryonic growth and development, and with growth and carcass characteristics of the resultant chicks. In the first step the effect of in ovo injectionofZAC on the expression of insulin-like growth factors (IGFs:IGF-I and IGF-I), myog...

متن کامل

The synpolydactyly homolog (spdh) mutation in the mouse – a defect in patterning and growth of limb cartilage elements

We have investigated the recessive mouse mutant synpolydactyly homolog (spdh) as a model for human synpolydactyly (SPD). As in human SPD, the spdh phenotype consists of central polydactyly, syndactyly and brachydactyly and is caused by the expansion of a polyalanine encoding repeat in the 5' region of the Hoxd13 gene. We performed a detailed phenotypic and functional analysis of spdh/spdh embry...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Mechanisms of Development

دوره 126  شماره 

صفحات  -

تاریخ انتشار 2009