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莱茵衣藻中的小眼和多眼点基因座定义了新的眼点光感受和组装调节剂。

Miniature- and Multiple-Eyespot Loci in Chlamydomonas reinhardtii Define New Modulators of Eyespot Photoreception and Assembly.

出版信息

G3 (Bethesda). 2011 Nov;1(6):489-98. doi: 10.1534/g3.111.000679. Epub 2011 Nov 1.

DOI:10.1534/g3.111.000679
PMID:22384359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3276157/
Abstract

The photosensory eyespot of the green alga Chlamydomonas reinhardtii is a model system for the study of organelle biogenesis and placement. Eyespot assembly and positioning are governed by several genetic loci that have been identified in forward genetic screens for phototaxis-defective mutants. These include the previously described miniature-eyespot mutant min1, the multiple-eyespot mutant mlt1, the eyeless mutants eye2 and eye3, and two previously uncharacterized eyespot mutants, min2 and mlt2. In this study, effects of miniature- and multiple-eyespot mutations and their combinations on the localization and expression levels of the rhodopsin photoreceptor channelrhodopsin-1 (ChR1) and the localization of the eyespot-assembly proteins EYE2 and EYE3 were examined. min2 mutants assemble a properly organized, albeit nonfunctional, eyespot that is slightly smaller than wild-type; however, combination of the min2 and mlt1 mutations resulted in drastic reduction of photoreceptor levels. Both stationary-phase mlt1 and mlt2 cells have supernumerary, mislocalized eyespots that exhibit partial or total dissociation of the eyespot layers. In these mutant strains, photoreceptor patches in the plasma membrane were never associated with pigment granule arrays in the chloroplast stroma unless EYE2 was present in the intervening envelope. The data suggest that MIN2 is required for the photoreceptive ability of the eyespot and that MLT2 plays a major role in regulating eyespot number, placement, and integrity.

摘要

莱茵衣藻的光感觉眼点是研究细胞器发生和定位的模型系统。眼点的组装和定位受几个遗传位点的控制,这些遗传位点已在前向遗传筛选中被确定为光趋性缺陷突变体。这些包括先前描述的小眼点突变体 min1、多眼点突变体 mlt1、无眼突变体 eye2 和 eye3,以及两个以前未被表征的眼点突变体 min2 和 mlt2。在这项研究中,研究了小眼点和多眼点突变及其组合对视紫红质光受体通道视紫红质-1 (ChR1)的定位和表达水平以及眼点组装蛋白 EYE2 和 EYE3 的定位的影响。min2 突变体组装了一个适当组织的、但不起作用的眼点,其大小略小于野生型;然而,min2 和 mlt1 突变的组合导致光受体水平的急剧降低。静止期 mlt1 和 mlt2 细胞都有多余的、定位错误的眼点,这些眼点的层部分或完全分离。在这些突变株中,质膜中的光受体斑从未与叶绿体基质中的色素颗粒排列相关联,除非在中间的包膜中有 EYE2 存在。这些数据表明 MIN2 是眼点感光能力所必需的,而 MLT2 在调节眼点数量、位置和完整性方面起着主要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/c402202783de/489f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/68dce075d090/489f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/d6668d3b4795/489f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/b6ee270d6962/489f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/1f4fc54a53c4/489f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/d50fffb307fd/489f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/e77d1fea8b6e/489f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/127cbc192ade/489f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/c402202783de/489f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/68dce075d090/489f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/d6668d3b4795/489f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/b6ee270d6962/489f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/1f4fc54a53c4/489f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/d50fffb307fd/489f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/e77d1fea8b6e/489f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/127cbc192ade/489f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/72ce/3276157/c402202783de/489f8.jpg

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