Racing against the clock: How flies regenerate just in time

被引：0

作者：

Box, Allison M. ^{[1
]}

Buttitta, Laura ^{[1
]}

机构：

[1] Univ Michigan, Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA

来源：

DEVELOPMENTAL CELL | 2021年 / 56卷 / 14期

关键词：

GROWTH;

D O I：

10.1016/j.devcel.2021.06.015

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

In this issue of Developmental Cell, Cohen et al. show that the Drosophila hindgut is a genetically tractable model for studying tissue regeneration. This tissue exhibits different regeneration strategies at different developmental times, demonstrating that the hindgut developmental clock, not tissue type, dictates the mode and capacity for regeneration.

引用

页码：2012 / 2013

页数：3

共 10 条

[1] Cohen E, 2021, DEV CELL, V56
[2] Fizzy-Related dictates A cell cycle switch during organ repair and tissue growth responses in the Drosophila hindgut
Cohen, Erez
Allen, Scott R.
Sawyer, Jessica K.
Fox, Donald T.
[J]. ELIFE, 2018, 7
[3] Secreted Peptide Dilp8 Coordinates Drosophila Tissue Growth with Developmental Timing
Colombani, Julien
Andersen, Ditte S.
Leopold, Pierre
[J]. SCIENCE, 2012, 336 (6081) : 582 - 585
[4] Mammalian endoreplication emerges to reveal a potential developmental timer
Gandarillas, Alberto
Molinuevo, Rut
Sanz-Gomez, Natalia
[J]. CELL DEATH AND DIFFERENTIATION, 2018, 25 (03) : 471 - 476
[5] Imaginal Discs Secrete Insulin-Like Peptide 8 to Mediate Plasticity of Growth and Maturation
Garelli, Andres
Gontijo, Alisson M.
Miguela, Veronica
Caparros, Esther
Dominguez, Maria
[J]. SCIENCE, 2012, 336 (6081) : 579 - 582
[6] Retinoids Regulate a Developmental Checkpoint for Tissue Regeneration in Drosophila
Halme, Adrian
Cheng, Michelle
Hariharan, Iswar K.
[J]. CURRENT BIOLOGY, 2010, 20 (05) : 458 - 463
[7] Jones L, 2000, DEVELOPMENT, V127, P4619
[8] Lehman DA, 1999, DEVELOPMENT, V126, P1793
[9] Changes in chromatin accessibility ensure robust cell cycle exit in terminally differentiated cells
Ma, Yiqin
McKay, Daniel J.
Buttitta, Laura
[J]. PLOS BIOLOGY, 2019, 17 (09)
[10] Notch-dependent fizzy-related/Hec1/Cdh1 expression is required for the mitotic-to-endocycle transition in Drosophila follicle cells
Schaeffer, V
Althauser, C
Shcherbata, HR
Deng, WM
Ruohola-Baker, H
[J]. CURRENT BIOLOGY, 2004, 14 (07) : 630 - 636

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