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Volume 60 - Tomato Genetics Cooperative - University of Florida

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Research Papers TGC REPORT VOLUME <strong>60</strong>, 2010<br />

Study <strong>of</strong> epidermal cell size <strong>of</strong> petals and stamens in tomato species and hybrids<br />

using confocal laser-scanning microscopy<br />

Christopher L<strong>of</strong>ty, Julian Smith, Pravda Stoeva-Popova<br />

Department <strong>of</strong> Biology, Winthrop <strong>University</strong>, Rock Hill SC 29733<br />

E-mail: stoevap@winthrop.edu<br />

Introduction<br />

The phenomenon <strong>of</strong> cytoplasmic male sterility (CMS) has been described and<br />

the genetics underlying the phenomemon studied in many species. Whether arising<br />

spontaneously, as the result <strong>of</strong> mutations, or through alloplasmic incompatibilities in<br />

interspecific crosses, the main effect <strong>of</strong> CMS is on the development <strong>of</strong> stamens and<br />

pollen, leading to aberrant stamens with no pollen or aborted pollen (Kaul 1988). Other<br />

changes correlated with the CMS phenotype are changes in the second whorl affecting<br />

petal size and color (Andersen 1963, 1964; Petrova et al. 1999; Farbos et al. 2001;<br />

Leino et al. 2003)<br />

In the tomato, CMS does not occur naturally. CMS has been reported in<br />

interspecies hybrids. Andersen (1963, 1964) reported the emergence and increase <strong>of</strong><br />

pollen abortion in F1 and backcrosses <strong>of</strong> the crosses between Solanum lycopersicum,<br />

S. cheesmaniiae (formerly L. chesmanii f. typicum and f. minor) or S. habrochaites<br />

(formerly L. hirsutum f. glabratum) used as pistillate parents and S. pennellii as the<br />

recurrent pollinating parent. Pleiotropic effects <strong>of</strong> the CMS phenotype included the<br />

reduction <strong>of</strong> anther length and size, and the lengthening <strong>of</strong> the filaments. The anther<br />

size was negatively correlated to the percent <strong>of</strong> aborted pollen.<br />

Similar results were observed by Valkova-Atchkova (1980) in crosses involving<br />

S. peruvianum as pistillate parent and S. pennellii and S. habrochaites (formerly L.<br />

hirsutum f. typicum) as pollinating parents. Further introgression <strong>of</strong> the nuclear genome<br />

<strong>of</strong> the recurrent parents confirmed the stability <strong>of</strong> the CMS phenotype over many<br />

generations (Petrova et al. 1999, Stoeva et al. 2007).<br />

As a preliminary step to dissecting morphological (and underlying genetic)<br />

changes occurring in the CMS phenotype, this study has focused on the comparative<br />

analysis <strong>of</strong> the size <strong>of</strong> epidermal cells from abaxial and adaxial sides <strong>of</strong> petals and<br />

stamens <strong>of</strong> mature flowers from CMS-pennellii line (0% stainable pollen), the isonuclear<br />

S. pennellii (100% pollen fertility), and the cultivated tomato S. lycopersicum.<br />

Materials and methods<br />

Plant material<br />

In the study the following genotypes were used: Solanum lycopersicum (cv.<br />

Merkurii), Solanum pennellii (LA716), and CMS-pennellii (CMS line) previously<br />

described in Petrova et al. (1998) and Radkova (2002). To determine the size <strong>of</strong> the<br />

epidermal cells, fully expanded flowers in stage 20 according to the classification <strong>of</strong><br />

Burkhin et al. (2003) were collected from plants grown in the same environmental<br />

58

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