1986
DOI: 10.1093/nar/14.10.4051
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Structure and expression of three light-harvesting chlorophyll a/b-binding protein genes in Arabidopsis thaliana

Abstract: The genome of Arabidopsis thaliana is exceedingly small, in part because it lacks the large middle repetitive DNA component characteristic of other plants. In this paper we have characterized a member of the low copy DNA component: the gene family for the light-harvesting chlorophyll a/b-protein. This gene family is unusual in that it contains far fewer members than the 7-16 coding sequences for this protein found in other plants. We used cross-hybridization with a Lemna gene encoding a light-harvesting chloro… Show more

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Cited by 240 publications
(193 citation statements)
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“…The CAB2-specific probe is a 22-base oligonucleotide from the specific RNA leader of the CAB2 transcript (Leutwiler et al, 1986), 5Ј-ATGACTAACTTGTGAG-TGAGA-3Ј. The CAB1 probe is a 42-base oligonucleotide from the CAB1 mRNA leader region, 5Ј-CAGCAC-AAAGTAAACGTTTAAGATTTGTTGTTGTAAGCCAA-3Ј.…”
Section: Rna Gel Blot Analysismentioning
confidence: 99%
See 1 more Smart Citation
“…The CAB2-specific probe is a 22-base oligonucleotide from the specific RNA leader of the CAB2 transcript (Leutwiler et al, 1986), 5Ј-ATGACTAACTTGTGAG-TGAGA-3Ј. The CAB1 probe is a 42-base oligonucleotide from the CAB1 mRNA leader region, 5Ј-CAGCAC-AAAGTAAACGTTTAAGATTTGTTGTTGTAAGCCAA-3Ј.…”
Section: Rna Gel Blot Analysismentioning
confidence: 99%
“…The alcohol dehydrogenase (ADH) gene probe is a 0.6-kb SalI-NotI fragment of the 194E11T7 expressed sequence tag clone, and the albumin (ALB) 2S gene probe is a 0.7-kb SalI-NotI fragment of the 107I7T7 expressed sequence tag clone. As loading control for total RNA, we used an 18S rDNA fragment cloned from Arabidopsis (Takahashi et al, 1995).The CAB2-specific probe is a 22-base oligonucleotide from the specific RNA leader of the CAB2 transcript (Leutwiler et al, 1986), 5Ј-ATGACTAACTTGTGAG-TGAGA-3Ј. The CAB1 probe is a 42-base oligonucleotide from the CAB1 mRNA leader region, 5Ј-CAGCAC-AAAGTAAACGTTTAAGATTTGTTGTTGTAAGCCAA-3Ј.…”
mentioning
confidence: 99%
“…Filter hybridizations were performed at 65OC in a solution containing 7% SDS, 500 mM NaH2P04, pH 7.2,1% BSA, and 1 mM EDTA. The DNA probes used are as follows: a 0.55-kb DNA fragment (generated by polymerase chain reaction) corresponding to the entire open reading frame of the Arabidopsis small subunit of ribulose-l,5-bisphosphate carboxylase rbcS gene (Krebbers et al, 1988); a 0.5-kb BamHI-Sstl DNA fragment corresponding to the coding region of the Arabidopsis chlorophyll alb (cab3) gene (Leutwiler et al, 1986); a 1.5-kb Hincll-ECORI DNA fragment containing the Arabidopsis ferredoxin type A (fedA) gene (Somers et al, 1990); a 1.2-kb Bglll-Xbal DNA fragment containing most of the coding region of a spinach chloroplast plastid @sbA) gene (Zurawski et al, 1982); and a 2-kb Hindlll fragment containing the entire p-glucuronidase (GUS) coding sequence used for the cabl promoter-GUS constructs (Deng et al, 1991). For all probes, -200 ng of each purified DNA fragment was labeled to high specific activity (-2 to 3 x 105 cpmlng DNA) by random oligomer priming, denatured by boiling for 5 min, and used for hybridization.…”
Section: Rna Analysismentioning
confidence: 99%
“…In Arabidopsis, several multiple loci exist for genes of Lhcb1 and Lhcb2. There are at least five (Lhcb1.1-Lhcb1.5) (AT1G29920, AT1G29910, AT1G29930, AT2G34430, AT2G34420), and three (Lhcb2.1-Lhcb2.3) (AT2G05100, AT2G05070, AT3G27690) multiple loci encoding Lhcb1 and Lhcb2 respectively in A. thaliana [3][4][5] (Table 1). The amino acid sequences of these individual Lhcb1 and Lhcb2 proteins are slightly different.…”
mentioning
confidence: 99%