Lung specific developmental expression of the Xenopus laevis surfactant protein C and B genes

被引:17
作者
Hyatt, Brian A.
Resnik, Ernesto R.
Johnson, Natalie S.
Lohr, Jamie L.
Cornfield, David N. [1 ]
机构
[1] Stanford Univ, Dept Pediat, Stanford, CA 94305 USA
[2] Univ Minnesota, Dept Pediat, Div Pediat Cardiol, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Pediat, Div Pediat Pulm & Crit Care Med, Minneapolis, MN 55455 USA
[4] Bethel Univ, St Paul, MN 55112 USA
关键词
surfactant proteins; Xenopus laevis; lung development;
D O I
10.1016/j.modgep.2006.05.001
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Efforts to characterize the mechanisms underlying early lung development have been confounded by the absence of a model that permits study of lung development prior to the onset of endodermal differentiation. Since Xenopus laevis development occurs in an extrauterine environment, we sought to determine whether the classical molecular markers of lung development and function, surfactant protein genes, are expressed in X. laevis. Surfactant protein C (SP-C) is a specific marker for lung development, expressed early in development and exclusively in the lung. Surfactant protein B (SP-B) expression is essential for life, as its absence results in neonatal death in mice and gene mutations have been associated with neonatal respiratory failure in humans. Here, we report the cloning of the first nonmammalian SP-C and SP-B genes (termed xSP-C and xSP-B) using the Xenopus model. The processed mature translated regions of both xSP-C and xSP-B have high homology with both human and mouse genes. xSP-C and xSP-B are both expressed throughout the lung of the X. laevis swimming tadpoles soon after the initiation of lung development as assessed by RT-PCR and whole mount in situ hybridization. The temporal expression patterns of xSP-C and xSP-B are consistent with the expression patterns in mammalian models of lung development. In both the tadpole and the adult X. laevis, xSP-C and xSP-B are expressed only in lung. Knowledge of the sequence and expression pattern of these two surfactant proteins in Xenopus might allow for use of this organism to study early lung development. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:8 / 14
页数:7
相关论文
共 25 条
[1]   The transformation of the model organism: a decade of developmental genetics [J].
Anderson, KV ;
Ingham, PW .
NATURE GENETICS, 2003, 33 (Suppl 3) :285-293
[2]  
BRUNO MA, 1995, AM J PHYSL L, V268
[3]  
Copland Ian, 2004, Paediatr Respir Rev, V5 Suppl A, pS259, DOI 10.1016/S1526-0542(04)90049-8
[4]   SEQUENCE, ONTOGENY, AND CELLULAR-LOCALIZATION OF MURINE SURFACTANT PROTEIN-B MESSENGER-RNA [J].
DAMOREBRUNO, MA ;
WIKENHEISER, KA ;
CARTER, JE ;
CLARK, JC ;
WHITSETT, JA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (01) :L40-L47
[5]   The comparative biology of pulmonary surfactant: past, present and future [J].
Daniels, CB ;
Orgeig, S .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY, 2001, 129 (01) :9-36
[6]   Xnkx-2.1:: a homeobox gene expressed during early forebrain, lung and thyroid development in Xenopus laevis [J].
Hollemann, T ;
Pieler, T .
DEVELOPMENT GENES AND EVOLUTION, 2000, 210 (11) :579-581
[7]  
Johnston SD, 2002, J EXP BIOL, V205, P415
[8]   TEMPORAL-SPATIAL DISTRIBUTION OF SP-B AND SP-C PROTEINS AND MESSENGER-RNAS IN DEVELOPING RESPIRATORY EPITHELIUM OF HUMAN LUNG [J].
KHOOR, A ;
STAHLMAN, MT ;
GRAY, ME ;
WHITSETT, JA .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1994, 42 (09) :1187-1199
[10]  
MEBAN C, 1973, J ANAT, V114, P235