Differential Expression of Distinct Members of Rho Family GTP-Binding Proteins during Neuronal Development: Identification ofRac1B, a New Neural-Specific Member of the Family
Differential Expression of Distinct Members of Rho Family GTP-Binding Proteins during Neuronal Development: Identification ofRac1B, a New Neural-Specific Member of the Family
复制标题
Rho 家族 GTP 结合蛋白不同成员在神经元发育过程中的差异表达:Rac1B(该家族新的神经特异性成员)的鉴定
作者:
M. Malosio;D. Gilardelli;Simona Paris;C. Albertinazzi;I. de Curtis
Previous studies on small GTP-binding proteins of the Rho family have revealed their involvement in the organization of cell actin cytoskeleton. The function of these GTPases during vertebrate development is not known. With the aim of understanding the possible role of these proteins during neuronal development, we have cloned and sequenced five members expressed in developing chick neural retinal cells. We have identified four chicken genes, cRhoA, cRhoB, cRhoC, and cRac1A, homologous to known human genes, and a novel Rac gene,cRac1B. Analysis of the distribution of four of the identified transcripts in chicken embryos shows for the first time high levels of expression of Rho family genes in the vertebrate developing nervous system, with distinct patterns of distribution for the different transcripts. In particular, cRhoA andcRac1A gene expression appeared ubiquitous in the whole embryo, and the cRhoB transcript was more prominent in populations of neurons actively extending neurites, whereas the newly identified cRac1B gene was homogeneously expressed only in the developing nervous system. Temporal analysis of the expression of the five genes suggests a correlation with the morphogenetic events occurring within the developing retina and the retinotectal pathway. Expression of an epitope-tagged cRac1B in retinal neurons showed a diffuse distribution of the protein in the cell body and along neurites. Taken as a whole, our results suggest important roles for ubiquitous and neural-specific members of the Rho family in the acquisition of the mature neuronal phenotype.
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影响因子:
--
作者:
G. Pfeifer;A. Riggs
通讯作者:
G. Pfeifer;A. Riggs
DOI:
10.1146/annurev.cb.07.110191.000443
发表时间:
1991
期刊:
Annual review of cell biology
影响因子:
--
作者:
Mecham,RP
通讯作者:
Mecham,RP
影响因子:
4.1
作者:
Gibson, RM;Wilson-Delfosse, AL
通讯作者:
Wilson-Delfosse, AL
影响因子:
3.4
作者:
Biscardi,JS;Cooper,NG;Maness,PF
通讯作者:
Maness,PF
DOI:
10.1242/dev.118.2.377
发表时间:
1993
期刊:
Development (Cambridge, England)
影响因子:
--
作者:
deCurtis,I;Reichardt,LF
通讯作者:
Reichardt,LF