You will be redirected to the new profile page automatically in 3 seconds. Please bookmark the correct page at http://asp.cumc.columbia.edu/facdb/profile_list.asp?DepAffil=Genetics&uni=elaufer/
Columbia University Medical Center Logobanner3

Faculty Profile

Ed Laufer

Address:
701 West 168th Street
Room 1130A
New York, NY 10032

Phone: 212-305-1756
Fax: 212-923-2090

elaufer@columbia.edu

 

Affiliations
Department of Genetics & Development


Training Activities

Integrated Program in Cellular, Molecular & Biophysical Studies
Graduate Program in Genetics & Development


Edward M. Laufer, PhD
Assistant Professor of Genetics & Development

Research Summary

MOLECULAR GENETIC ANALYSIS OF VERTEBRATE PATTERN FORMATION

Our lab studies pattern formation during vertebrate development, using the embryonic chick limb bud as our primary model system. We use a combination of surgical manipulations and molecular genetic approaches to explore how limbs develop.

Growth and patterning of the limb are coordinately controlled by multiple inductive signals that impinge on the developmentally plastic tissue of the early limb bud. These signals are produced by tightly regulated signaling centers, located at specific positions within the bud. We wish to understand what these signals are, how they exert their effects on the fate and arrangement of limb tissues, and how the signaling centers are themselves controlled. Two representative projects are described below.

The apical ectodermal ridge is one signaling center that is a specialized epithelial structure located at the tip of the limb bud. The ridge signals to the underlying mesenchyme through the production of fibroblast growth factors, FGFs, and promotes limb outgrowth and patterning. This process is complex and involves several interactive regulatory circuits between the ridge and the mesenchyme. Numerous genes expressed in the mesenchyme and implicated in these processes are regulated by ridge signals. These genes are expressed in overlapping domains that extend different distances from the ridge. Using a retrovirally mediated form of clonal analysis, we are investigating whether these genes are regulated directly by FGF signals, and if so, if there are distinct signaling thresholds that control their differential expression patterns.

While the signals produced by some signaling centers are known, many have not been molecularly identified. In another project, we are screening genes encoding novel secreted factors for expression patterns suggestive of important inductive functions. We have identified one gene that might regulate dorso-ventral limb pattern. Later in development it might also control developmentally significant apoptosis, such as that which leads to selective elimination of interdigital tissue. Experiments testing these possibilities through the analysis of mutant animals, as well as by gene misexpression are under way.


Selected Publications


1.  Firulli BA, Krawchuk D, Centonze VE,  Vargesson N, Virshup DM, Conway SJ,  Cserjesi P, Laufer E, Firulli AB. (2005).  Altered  Twist1 and Hand2 dimerization is associated with Saethre-Chotzen syndrome and limb abnormalities. Nat Genet. 37(4): 373-381.

2.  Vasiliauskas D, Laufer E, Stern CD. (2003). A role for hairy1 in regulating chick limb bud growth.  Dev Biol. 262(1): 94-106.

3. Liu JP, Laufer E, Jessell TM. (2001). Assigning  the positional identity of spinal motor neurons:  rostrocaudal patterning of Hox-c expression by FGFs, Gfd11, and retinoids. Neuron. 32(6): 997-1012.

4. Vargesson N, Laufer E. (2001). Smad7 misexpression during embryonic angiogenesis causes vascular dilation and malformations independently of vascular smooth muscle cell function. Dev Biol. 240(2): 499-516.

5. Vargesson N, Luria V, Messina I, Erskine L, Laufer E. (2001). Expression patterns of Slit and Robo family members during vertebrate limb development. Mech Dev. 106(1-2):175-180.





top

CUMC Home | At Columbia University | Affiliated with New York-Presbyterian Hospital | Genetics & Development | Comments