TY - JOUR
T1 - A role for Lin-28 in growth and metamorphosis in Drosophila melanogaster
AU - González-Itier, Sergio
AU - Contreras, Esteban G.
AU - Larraín, Juan
AU - Glavic, Álvaro
AU - Faunes, Fernando
N1 - Funding Information:
We would like to thank J. Ewer for critical reading of the manuscript. Stocks obtained from the Bloomington Drosophila Stock Center (NIH P40OD018537) were used in this study. We thank A. Brand and the Developmental Studies Hybridoma Bank (DSHB) for antibodies, and T. Heino and N. Sokol for fly stocks. This work was funded by the following Grants: FONDECYT Postdoctorado 3160412 (E.G.C.), CONICYT PIA ACT1401 and FONDAP #15090007 (A.G), CARE Chile UC-Centro de Envejecimiento y Regeneraci?n PFB 12/2007, MINREB RC120003 and FONDECYT 1141162 (J.L.), FONDECYT Iniciaci?n 11130564 and Universidad Andres Bello #DI-29-17/RG (F.F.).
Funding Information:
We would like to thank J. Ewer for critical reading of the manuscript. Stocks obtained from the Bloomington Drosophila Stock Center (NIH P40OD018537) were used in this study. We thank A. Brand and the Developmental Studies Hybridoma Bank (DSHB) for antibodies, and T. Heino and N. Sokol for fly stocks. This work was funded by the following Grants: FONDECYT Postdoctorado 3160412 (E.G.C.), CONICYT PIA ACT1401 and FONDAP #15090007 (A.G), CARE Chile UC-Centro de Envejecimiento y Regeneración PFB 12/2007 , MINREB RC120003 and FONDECYT 1141162 (J.L.), FONDECYT Iniciación 11130564 and Universidad Andres Bello #DI-29-17/RG (F.F.).
Funding Information:
We would like to thank J. Ewer for critical reading of the manuscript. Stocks obtained from the Bloomington Drosophila Stock Center (NIH P40OD018537) were used in this study. We thank A. Brand and the Developmental Studies Hybridoma Bank (DSHB) for antibodies, and T. Heino and N. Sokol for fly stocks. This work was funded by the following Grants: FONDECYT Postdoctorado 3160412 (E.G.C.), CONICYT PIA ACT1401 and FONDAP #15090007 (A.G), CARE Chile UC-Centro de Envejecimiento y Regeneración PFB 12/2007, MINREB RC120003 and FONDECYT 1141162 (J.L.), FONDECYT Iniciación 11130564 and Universidad Andres Bello #DI-29-17/RG (F.F.).
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/6/14
Y1 - 2018/6/14
N2 - Insect metamorphosis has been a classic model to understand the role of hormones in growth and timing of developmental transitions. In addition to hormones, transitions in some species are regulated by genetic programs, such as the heterochronic gene network discovered in C. elegans. However, the functional link between hormones and heterochronic genes is not clear. The heterochronic gene lin-28 is involved in the maintenance of stem cells, growth and developmental timing in vertebrates. In this work, we used gain-of-function and loss-of-function experiments to study the role of Lin-28 in larval growth and the timing of metamorphosis of Drosophila melanogaster. During the late third instar stage, Lin-28 is mainly expressed in neurons of the central nervous system and in the intestine. Loss-of-function lin-28 mutant larvae are smaller and the larval-to-pupal transition is accelerated. This faster transition correlates with increased levels of ecdysone direct target genes such as Broad-Complex (BR-C) and Ecdysone Receptor (EcR). Overexpression of Lin-28 does not affect the timing of pupariation but most animals are not able to eclose, suggesting defects in metamorphosis. Overexpression of human Lin-28 results in delayed pupariation and the death of animals during metamorphosis. Altogether, these results suggest that Lin-28 is involved in the control of growth during larval development and in the timing and progression of metamorphosis.
AB - Insect metamorphosis has been a classic model to understand the role of hormones in growth and timing of developmental transitions. In addition to hormones, transitions in some species are regulated by genetic programs, such as the heterochronic gene network discovered in C. elegans. However, the functional link between hormones and heterochronic genes is not clear. The heterochronic gene lin-28 is involved in the maintenance of stem cells, growth and developmental timing in vertebrates. In this work, we used gain-of-function and loss-of-function experiments to study the role of Lin-28 in larval growth and the timing of metamorphosis of Drosophila melanogaster. During the late third instar stage, Lin-28 is mainly expressed in neurons of the central nervous system and in the intestine. Loss-of-function lin-28 mutant larvae are smaller and the larval-to-pupal transition is accelerated. This faster transition correlates with increased levels of ecdysone direct target genes such as Broad-Complex (BR-C) and Ecdysone Receptor (EcR). Overexpression of Lin-28 does not affect the timing of pupariation but most animals are not able to eclose, suggesting defects in metamorphosis. Overexpression of human Lin-28 results in delayed pupariation and the death of animals during metamorphosis. Altogether, these results suggest that Lin-28 is involved in the control of growth during larval development and in the timing and progression of metamorphosis.
KW - Developmental transitions
KW - Ecdysone signaling
KW - Growth
KW - Lin-28
KW - Metamorphosis
KW - Pupariation
UR - http://www.scopus.com/inward/record.url?scp=85048772514&partnerID=8YFLogxK
U2 - 10.1016/j.mod.2018.06.002
DO - 10.1016/j.mod.2018.06.002
M3 - Article
AN - SCOPUS:85048772514
SN - 0925-4773
VL - 154
SP - 107
EP - 115
JO - Mechanisms of Development
JF - Mechanisms of Development
ER -