TY - JOUR
T1 - Partial cloning and sequencing of chick fibrillin-1 cDNA
AU - Zhou, Guimei
AU - Price, Christopher E.
AU - Rosenquist, Thomas H.
AU - Gadson, Preston F.
AU - Godfrey, Maurice
N1 - Funding Information:
This work was supported in part by a grant f'om the National Heart, Lung, and Blood Institute of the National Institutes of Health HL48126 (M. G.), National Marian Foundation, USA, March of Dimes Birth Defects Foundation (FY98-0522), and the American Heart Association, Heartland Affiliate (9807991S). M. G. is an Established Investigator of the American Heart Association (funding was contributed in part by the AHA Florida Affiliate). The authors wish to thank Chad Price for expert computational assistance, Joe Edwards for his graphics expex~ise, and Dr. Angie Rizzino for advice and support.
PY - 2000/1
Y1 - 2000/1
N2 - The recent identification of numerous matrix genes and gene products has allowed a detailed examination of their roles in development. Two of these extracellular matrix proteins, fibrillin-1 and fibrillin-2, are components of the elastin-associated microfibrils. Given what is known about the distribution of the fibrillins in normal tissues and the abnormalities that result when mutations occur, a basic hypothesis has emerged: fibrillin-1 is primarily responsible for load bearing and providing structural integrity, whereas fibrillin-2 may be a director of elastogenesis. Nevertheless, examination of phenotypes in disorders caused by mutations in fibrillin-1 or fibrillin-2 suggests some common functions. To better understand these similar and diverse roles, it would be helpful to examine these proteins during chick development. To accomplish this goal, it is first necessary to characterize the chick homologs of the known fibrillins. In this study, the partial chick FBN1 cDNA was identified by polymerase chain reaction-aided cloning as a first step toward elucidating these goals. Sequence analysis indicated that there is striking conservation between chick and mammalian fibrillin-1 at the DNA and protein levels. Antisense and sense riboprobes were synthesized and used in in situ hybridization in stage 14 chick embryos and high levels of FBN1 transcripts were observed in the heart.
AB - The recent identification of numerous matrix genes and gene products has allowed a detailed examination of their roles in development. Two of these extracellular matrix proteins, fibrillin-1 and fibrillin-2, are components of the elastin-associated microfibrils. Given what is known about the distribution of the fibrillins in normal tissues and the abnormalities that result when mutations occur, a basic hypothesis has emerged: fibrillin-1 is primarily responsible for load bearing and providing structural integrity, whereas fibrillin-2 may be a director of elastogenesis. Nevertheless, examination of phenotypes in disorders caused by mutations in fibrillin-1 or fibrillin-2 suggests some common functions. To better understand these similar and diverse roles, it would be helpful to examine these proteins during chick development. To accomplish this goal, it is first necessary to characterize the chick homologs of the known fibrillins. In this study, the partial chick FBN1 cDNA was identified by polymerase chain reaction-aided cloning as a first step toward elucidating these goals. Sequence analysis indicated that there is striking conservation between chick and mammalian fibrillin-1 at the DNA and protein levels. Antisense and sense riboprobes were synthesized and used in in situ hybridization in stage 14 chick embryos and high levels of FBN1 transcripts were observed in the heart.
KW - Chick
KW - Development
KW - Extracellular matrix
KW - Fibrillin
KW - In situ hybridization
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U2 - 10.1290/1071-2690(2000)036<0019:PCASOC>2.3.CO;2
DO - 10.1290/1071-2690(2000)036<0019:PCASOC>2.3.CO;2
M3 - Article
C2 - 10691037
AN - SCOPUS:0034069759
SN - 1071-2690
VL - 36
SP - 19
EP - 25
JO - In Vitro Cellular and Developmental Biology - Animal
JF - In Vitro Cellular and Developmental Biology - Animal
IS - 1
ER -