Seasonal variation in the nuclear genome size of ray cells in the vascular cambium of Fraxinus americana

1995 ◽  
Vol 93 (2) ◽  
pp. 305-311 ◽  
Author(s):  
Y. Zhong ◽  
E. J. Mellerowicz ◽  
A. D. Lloyd ◽  
V. Leinhos ◽  
R. T. Riding ◽  
...  
1995 ◽  
Vol 93 (2) ◽  
pp. 305-311 ◽  
Author(s):  
Y. Zhong ◽  
E. J. Mellerowicz ◽  
A. D. Lloyd ◽  
V. Leinhos ◽  
R. T. Riding ◽  
...  

2017 ◽  
Vol 01 (02) ◽  
pp. 108-120 ◽  
Author(s):  
Nick Lane

All complex life on Earth is composed of ‘eukaryotic’ cells. Eukaryotes arose just once in 4 billion years, via an endosymbiosis — bacteria entered a simple host cell, evolving into mitochondria, the ‘powerhouses’ of complex cells. Mitochondria lost most of their genes, retaining only those needed for respiration, giving eukaryotes ‘multi-bacterial’ power without the costs of maintaining thousands of complete bacterial genomes. These energy savings supported a substantial expansion in nuclear genome size, and far more protein synthesis from each gene.


2008 ◽  
Vol 276 (3-4) ◽  
pp. 209-217 ◽  
Author(s):  
Itayguara Ribeiro da Costa ◽  
Marcelo Carnier Dornelas ◽  
Eliana Regina Forni-Martins

2005 ◽  
Vol 21 (2) ◽  
pp. 145-150
Author(s):  
T. K. Kyrylenko ◽  
O. I. Martynenko ◽  
O. G. Alkhimova

2018 ◽  
Vol 221 (3) ◽  
pp. 1609-1618 ◽  
Author(s):  
Fan Qiu ◽  
Eric J. Baack ◽  
Kenneth D. Whitney ◽  
Dan G. Bock ◽  
Hannah M. Tetreault ◽  
...  

Euphytica ◽  
2008 ◽  
Vol 164 (1) ◽  
pp. 221-230 ◽  
Author(s):  
Guadalupe Palomino ◽  
Laura Trejo Hernández ◽  
Eulogio de la Cruz Torres

1996 ◽  
Vol 74 (2) ◽  
pp. 290-298 ◽  
Author(s):  
A. D. Lloyd ◽  
C. H. A. Little ◽  
E. J. Mellerowicz ◽  
R. T. Riding

The relationship between nuclear genome size, measured cytophotometrically, and relative ribosomal RNA gene (rDNA) content, determined as the ratio of the hybridization signals from a 25S rRNA gene probe and a randomly labelled total genomic DNA probe, was investigated in cambial region cells of balsam fir (Abies balsamea (L.) Mill.) shoots during the onset of dormancy and the transition between the dormancy stages of rest and quiescence. The dormancy status was manipulated by exposing potted trees for 13 weeks, starting August 14 when the cambium was still active, to one of the following environments: (i) the declining temperature and photoperiod of the natural environment (denoted N-N), (ii) simulated natural temperature and 15-h photoperiod (sN-15), (iii) simulated natural temperature and 8-h photoperiod (sN-8), and (iv) warm temperature and 15-h photoperiod (sN-15). On November 12, the trees were transferred to a greenhouse having environmental conditions favorable for growth to assess their ability to reactivate. The entire activity –rest–quiescence transition occurred in the N-N environment and was associated with an increase in nuclear genome size and a decrease in the relative rDNA content. The sN-8 environment also induced the transition but not completely, and the associated increase and decrease in nuclear genome size and relative rDNA content, respectively, were smaller than in the N-N environment. The sN-15 environment delayed the onset of rest, inhibited the changeover to quiescence, increased then decreased the nuclear genome size, and did not affect the relative rDNA content. The W-15 environment, which induced budbreak and the formation of a false ring, also prevented the rest–quiescence transition and transiently increased the nuclear genome size without altering the relative rDNA content. The data suggest that the normal rest–quiescence progression in shoot cambial cells is associated with an increase in nuclear genome size, which is caued by amplification of a fraction that is not rDNA but is recognized by our genomic probe. Keywords: dormancy, genome size, ribosomal RNA genes, vascular cambium.


IAWA Journal ◽  
1991 ◽  
Vol 12 (2) ◽  
pp. 177-185 ◽  
Author(s):  
T. O. Siddiqi

In Ficus religiosa (Moraceae) extension and radial growth occurs in late July and early August, respectively, under the local climate of Aligarh. The derivative tissue differentiates into xylem and phloem simultaneously in August. The phloem production stops late in August, restarts early October and then continues up to November. The xylogenesis continues up to November without interruption. Formation of the precursor phloem is observed in March. Cell size and the relative proportion of fusiform and ray initials vary with season.


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