scholarly journals Determination of steady-state mRNA levels of individual chlorophyll a/b binding protein genes of the tomato cab gene family

1991 ◽  
Vol 230 (3) ◽  
pp. 413-422 ◽  
Author(s):  
Birgit Piechulla ◽  
Jan-Wolfhard Kellmann ◽  
Eran Pichersky ◽  
Egbert Schwartz ◽  
Hans-Heinrich Förster
2003 ◽  
Vol 6 (1) ◽  
pp. 33-39 ◽  
Author(s):  
Telse Meyer ◽  
Michael Hust ◽  
Jürgen Marquardt ◽  
Wolfgang E. Krumbein ◽  
Erhard Rhiel

1995 ◽  
Vol 28 (6) ◽  
pp. 1133-1141 ◽  
Author(s):  
Yuriko Osakabe ◽  
Keishi Osakabe ◽  
Shinya Kawai ◽  
Yoshihiro Katayama ◽  
Noriyuki Morohoshi

Genome ◽  
1994 ◽  
Vol 37 (1) ◽  
pp. 166-172 ◽  
Author(s):  
John W. Barrett ◽  
Robin N. Beech ◽  
Bruce P. Dancik ◽  
Curt Strobeck

A type I cab gene encoding chlorophyll a and b binding protein from lodgepole pine (Pinus contorta Dougl., var. latifolia (Engelm.)) has been isolated and sequenced. The gene encodes a proposed 40 amino acid transit peptide and a 234 amino acid mature CAB polypeptide. There is no evidence of an intron and examination of the type-specific amino acids confirm this to be a photosystem II type I cab gene. The coding region is highly conserved with a similar gene from Scots pine, the homology extending into the 5′ and 3′ untranslated regions. Sequence comparison of the 1-kb region upstream of the translation start codon from the lodgepole pine cab gene exhibited little similarity to identified regulatory regions in pea, tobacco, wheat, and Arabidopsis cab genes. The cab gene, which is 62% G + C rich, is surrounded by 70–75% A + T rich regions, which may confer some regulatory feature on its expression.Key words: chlorophyll a/b binding protein, gymnosperm, lodgepole pine, photosystem II type I cab gene.


1999 ◽  
Vol 22 (3) ◽  
pp. 261-272 ◽  
Author(s):  
V Dunaiski ◽  
FR Dunshea ◽  
PE Walton ◽  
C Goddard

The effect of short-term GH treatment on steady-state insulin-like growth factor binding protein-3 (IGFBP-3) mRNA levels in liver, kidney, longissimus dorsi muscle, stomach and jejunum was examined in pigs. Ten female crossbred pigs were allocated to either saline or GH (70 microg/kg/day) treatment by subcutaneous injection for 4 days. They were allowed to feed ad libitum, and were weighed daily. At the end of the treatment period, the pigs were slaughtered and samples of liver, kidney, skeletal muscle, stomach and jejunum were collected and total RNA was extracted. Steady-state levels of IGFBP-3 mRNA were quantified by RNase protection assay and were compared with the level of IGF-I class 1 and class 2 transcripts. IGFBP-3 mRNA increased in response to GH in both liver and kidney, but not in the other tissues sampled. Hepatic IGF-I mRNA responded to short-term GH treatment with a fourfold increase in IGF-I class 1 mRNA and an eightfold increase in IGF-I class 2 mRNA, which was liver specific. IGF-I class 1 mRNA was not responsive to GH treatment in other tissues. The short-term nature of this treatment suggests that the increase in hepatic IGFBP-3 and IGF-I transcripts is a relatively early response to treatment with GH, and that the increase in plasma concentrations of IGFBP-3 in response to GH are derived from the liver, the kidney, or both.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Xian-Wen Li ◽  
Yu-Lin Zhu ◽  
Chu-Yan Chen ◽  
Zhi-Juan Geng ◽  
Xiang-Yong Li ◽  
...  

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