Distinct mechanisms triggering glial differentiation in Drosophila thoracic and abdominal Neuroblasts 6-4

被引:19
作者
Akiyama-Oda, Y
Hotta, Y
Tsukita, S
Oda, H
机构
[1] Kyoto Univ, Fac Med, Dept Cell Biol, Sakyo Ku, Kyoto 6068501, Japan
[2] Japan Sci & Technol Corp, Exploratory Res Adv Technol, Tsukita Cell Axis Project, Shimogyo Ku, Kyoto 6008813, Japan
[3] Natl Inst Genet, Shizuoka 4118540, Japan
关键词
neuroblast; glia; neuron; cell division; gcm; repo; string; pebble; cyclin A; Drosophila;
D O I
10.1006/dbio.2000.9727
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Neurons and glia are produced in stereotyped patterns after neuroblast cell division during development of the Drosophila central nervous system. The first cell division of thoracic neuroblast 6-4 (NB6-4T) is asymmetric, giving rise to a glial precursor cell and a neuronal precursor cell. In contrast, abdominal NB6-4 (NB6-4A) divides symmetrically to produce two glial cells. To understand the relationship between cell division and glia-neuron cell fate determination, we examined and compared the effects of known cell division mutations on the NB6-4T and NB6-4A lineages. Based on observation of expression of glial fate determination and early glial differentiation genes, the onset of glial differentiation occurred in NB6-4A but not in NB6-4T when both cell cycle progression and cytokinesis were genetically arrested. On the other hand, glial differentiation started in both lineages when cytokinesis was blocked with intact cell cycle progression. These results showed that NB6-4T, but not NB6-4A, requires cell cycle progression for acquisition of glial fate, suggesting that distinct mechanisms trigger glial differentiation in the different lineages. (C) 2000 Academic Press.
引用
收藏
页码:429 / 439
页数:11
相关论文
共 48 条
[1]
The gcm-motif: A novel DNA-binding motif conserved in Drosophila and mammals [J].
Akiyama, Y ;
Hosoya, T ;
Poole, AM ;
Hotta, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14912-14916
[2]
Alteration of cell fate by ectopic expression of Drosophila glial cells missing in non-neural cells [J].
Akiyama-Oda, Y ;
Hosoya, T ;
Hotta, Y .
DEVELOPMENT GENES AND EVOLUTION, 1998, 208 (10) :578-585
[3]
Akiyama-Oda Y, 1999, DEVELOPMENT, V126, P1967
[4]
Ashburner M., 1989, DROSOPHILA LAB MANUA
[5]
The embryonic central nervous system lineages of Drosophila melanogaster .1. Neuroblast lineages derived from the ventral half of the neuroectoderm [J].
Bossing, T ;
Udolph, G ;
Doe, CQ ;
Technau, GM .
DEVELOPMENTAL BIOLOGY, 1996, 179 (01) :41-64
[6]
BRAND AH, 1993, DEVELOPMENT, V118, P401
[7]
NEW NEUROBLAST MARKERS AND THE ORIGIN OF THE ACC/PCC NEURONS IN THE DROSOPHILA CENTRAL-NERVOUS-SYSTEM [J].
BROADUS, J ;
SKEATH, JB ;
SPANA, EP ;
BOSSING, T ;
TECHNAU, G ;
DOE, CQ .
MECHANISMS OF DEVELOPMENT, 1995, 53 (03) :393-402
[8]
DROSOPHILA SPECTRIN .2. CONSERVED FEATURES OF THE ALPHA-SUBUNIT ARE REVEALED BY ANALYSIS OF CDNA CLONES AND FUSION PROTEINS [J].
BYERS, TJ ;
DUBREUIL, R ;
BRANTON, D ;
KIEHART, DP ;
GOLDSTEIN, LSB .
JOURNAL OF CELL BIOLOGY, 1987, 105 (05) :2103-2110
[9]
CAMPBELL G, 1994, DEVELOPMENT, V120, P2957
[10]
CHULAGRAFF Q, 1991, DEVELOPMENT, P79