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拟南芥损伤 DNA 结合蛋白 1B(DDB1B)与 DDB1A、DET1 和 COP1 的遗传相互作用。

Genetic interactions of Arabidopsis thaliana damaged DNA binding protein 1B (DDB1B) with DDB1A, DET1, and COP1.

机构信息

Department of Biological Sciences, University of Manitoba, Winnipeg, MB, Canada R3T 2N2.

出版信息

G3 (Bethesda). 2013 Mar;3(3):493-503. doi: 10.1534/g3.112.005249. Epub 2013 Mar 1.

DOI:10.1534/g3.112.005249
PMID:23450167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3583456/
Abstract

Damaged DNA Binding protein 1 (DDB1)-CULLIN4 E3 ubiquitin ligase complexes have been implicated in diverse biological processes in a range of organisms. Arabidopsis thaliana encodes two homologs of DDB1, DDB1A, and DDB1B. In this study we use a viable partial loss of function allele of DDB1B, ddb1b-2, to examine genetic interactions with DDB1A, DET1 and COP1. Although the ddb1b-2 ddb1a double mutant is lethal, ddb1a ddb1b-2/+ and ddb1b-2 ddb1a/+ heterozygotes exhibit few developmental phenotypes but do exhibit decreased tolerance of ultraviolet light. In addition, germination in ddb1a and ddb1a ddb1b-2/+ was found to be sensitive to salt and mannitol, and both DDB1 single mutants as well as the heterozygotes exhibited heat sensitivity. DE-ETIOLATED1 (DET1) and CONSTITUTIVE PHOTOMORPHOGENIC1 (COP1) are negative regulators of light development which interact with DDB1-CUL4 complexes. Although ddb1a strongly enhances det1 phenotypes in both dark- and light-grown seedlings, ddb1b-2 weakly enhanced the det1 short hypocotyl phenotype in the dark, as well as enhancing anthocyanin levels and suppressing the det1 low chlorophyll phenotype in light-grown seedlings. In adults, ddb1a suppresses det1 early flowering and enhances the det1 dwarf phenotype. A similar trend was observed in ddb1b-2 det1 double mutants, although the effects were smaller in magnitude. In cop1 mutants, ddb1b-2 enhanced the cop1-4 short hypocotyl phenotype in dark and light, enhanced anthocyanin levels in cop1-1 in the light, but had no effect in adults. Thus the requirement for DDB1B varies in the course of development, from COP1-specific effects in hypocotyls to DET1-specific in adults.

摘要

受损的 DNA 结合蛋白 1(DDB1)-CUL4 E3 泛素连接酶复合物在多种生物体的多种生物学过程中都有涉及。拟南芥编码两种 DDB1 同源物,DDB1A 和 DDB1B。在这项研究中,我们使用 DDB1B 的一种可行的部分功能丧失等位基因 ddb1b-2,来研究与 DDB1A、DET1 和 COP1 的遗传相互作用。尽管 ddb1b-2 ddb1a 双突变体是致死的,但 ddb1a ddb1b-2/+ 和 ddb1b-2 ddb1a/+ 杂合体表现出很少的发育表型,但对紫外线的耐受性降低。此外,在 ddb1a 和 ddb1a ddb1b-2/+中发现发芽对盐和甘露醇敏感,并且 DDB1 单突变体以及杂合体都表现出对热的敏感性。DE-ETIOLATED1(DET1)和 CONSTITUTIVE PHOTOMORPHOGENIC1(COP1)是光发育的负调节剂,与 DDB1-CUL4 复合物相互作用。尽管 ddb1a 在黑暗和光照条件下的幼苗中强烈增强了 det1 表型,但 ddb1b-2 仅在黑暗中弱增强了 det1 短下胚轴表型,同时增强了花青素水平并抑制了光照条件下幼苗的 det1 低叶绿素表型。在成体中,ddb1a 抑制 det1 早花并增强 det1 矮化表型。在 ddb1b-2 det1 双突变体中观察到类似的趋势,尽管效应的幅度较小。在 cop1 突变体中,ddb1b-2 增强了黑暗和光照条件下 cop1-4 的短下胚轴表型,增强了光照条件下 cop1-1 的花青素水平,但在成体中没有影响。因此,在发育过程中,DDB1B 的需求因 COP1 在下胚轴中的特异性作用到 DET1 在成体中的特异性作用而有所不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/e4e3bd22ebf6/493f9.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/60c40201c2f3/493f4.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/e4e3bd22ebf6/493f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/bf8553cd31f7/493f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/9327a15b1bbe/493f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/8cd5a66cde4d/493f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/60c40201c2f3/493f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/9a9d6c2e5f23/493f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/29f5d04f8119/493f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/b1b71ce451ef/493f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/4d42a3bc100d/493f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f14/3583456/e4e3bd22ebf6/493f9.jpg

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